IO2 SPHER(MANGOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR,IO2 TORIC (MANGOFILCON A) SOFT (HYDROPHILIC)
K133079 · Alden Optical Labs., Inc. · LPL · Dec 17, 2013 · Ophthalmic
Device Facts
Record ID
K133079
Device Name
IO2 SPHER(MANGOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR,IO2 TORIC (MANGOFILCON A) SOFT (HYDROPHILIC)
Applicant
Alden Optical Labs., Inc.
Product Code
LPL · Ophthalmic
Decision Date
Dec 17, 2013
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 886.5925
Device Class
Class 2
Indications for Use
The iO2 Sphere (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of myopia and hyperopia in aphakic or non-aphakic patients with nondiseased eyes who exhibit no more than 2.00 D of astigmatism and can obtain satisfactory visual acuity in a power range of +30.00 to -30.00 D. The ASTERA Multifocal iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of presbyopia in myopic and hyperopic eyes in aphakic or non-aphakic patients with non-diseased eyes who exhibit no more than 2.00 D of astigmatism and can obtain satisfactory visual acuity in a power range of +30.00 to -30.00 D and have near add requirements up to 3.25 D. The iO2Toric (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of refractive ametropia (myopia, and astigmatism) in aphakic or non- aphakic persons with non diseased eyes in a spherical power range of +30.00 to -30.00 D and a cylinder power range up to -10.0D. The ASTERA Multifocal Toric iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of presbyopia in myopic, hyperopic and astigmatic aphakic or non- aphakic patients with non-diseased eyes in a spherical power range of +30.00 to -30.00 D, a cylinder power range up to -10.00 D and an add requirement up to 3.25 D. iO2 lenses may be disinfected using chemical (not heat) disinfecting systems.
Device Story
iO2 contact lenses are lathe-cut, hemispheric flexible shells made of mangofilcon A (51% copolymer, 49% water). Available in spherical, multifocal, toric, and multifocal-toric designs. Lenses are plasma-treated in dry state to improve surface properties. Used for daily wear to correct refractive errors. Prescribed by eye care professionals; patient-worn. Benefits include vision correction and handling convenience via optional visibility tints. UV-blocking versions available. Disinfection requires chemical systems; heat disinfection contraindicated.
Clinical Evidence
No clinical data. Substantial equivalence supported by non-clinical performance testing, including chemical composition, purity, shelf life, leachability, biocompatibility, preservative uptake, color/light transmittance, refractive index, water content, oxygen transmissibility, specific gravity, and mechanical/hardness testing.
Technological Characteristics
Material: Mangofilcon A (non-ionic hydrophilic copolymer). Water content: 49%. Dk: 49 (Fatt units). Refractive index: 1.413 (hydrated). Plasma treated. Lathe-cut manufacturing. Available with/without UV absorber. Visibility tints (Blue/Aqua) optional. Shore D hardness ≥ 83.
Indications for Use
Indicated for correction of myopia, hyperopia, astigmatism, and presbyopia in aphakic or non-aphakic patients with non-diseased eyes. Power ranges: sphere +30.00D to -30.00D; cylinder up to -10.00D; add up to 3.25D.
Regulatory Classification
Identification
A soft (hydrophilic) contact lens is a device intended to be worn directly against the cornea and adjacent limbal and scleral areas of the eye to correct vision conditions or act as a therapeutic bandage. The device is made of various polymer materials the main polymer molecules of which absorb or attract a certain volume (percentage) of water.
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K133079
Image /page/0/Picture/1 description: The image shows a logo for Alden Optical. The logo consists of a stylized "A" shape above the words "ALDEN" and "OPTICAL", which are stacked vertically. The logo is black and white and has a slightly distressed or textured appearance.
DEC 1 7 2013
## 510(k) SUMMARY OF SAFETY AND EFFECTIVENESS
. ·
#### I. Submitter Information
| 510(k) Owner: | Alden Optical Laboratories, Inc.<br>6 Lancaster Pkwy<br>Lancaster, NY 14086 USA |
|---------------|---------------------------------------------------------------------------------|
|---------------|---------------------------------------------------------------------------------|
- Contact Person: Mr. Charley Creighton 716-937-9181 (office) 716-937-3303 (fax)
| Consultant &<br>Submission<br>Correspondent: | Kevin Randall, Principal Consultant<br>ComplianceAcuity, Inc.<br>Golden, CO 80403<br>(303) 828-0844 (direct)<br>(303) 828-0835 (fax)<br>Email: info@complianceacuity.com |
|----------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
|----------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
Date Summary September 27, 2013 Prepared:
#### II. Name of Device
| | Trade Name: iO2 (mangofilcon A) Soft (hydrophilic) | | |
|------------------------------------|-------------------------------------------------------|--|--|
| | Contact Lens for Daily Wear | | |
| | Common/Usual Name: Soft (hydrophilic) contact lens | | |
| | Classification Name: Lenses, Soft Contact, Daily Wear | | |
| USAN (generic name): Mangofilcon A | | | |
510(k) Summary Page I of 5
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Image /page/1/Picture/0 description: The image shows a logo for Alden Optical. The logo consists of a stylized triangle shape above the words "ALDEN OPTICAL". The triangle shape has a small triangle in the center. The text and shapes are black and the background is white.
#### III. Device Description & Technological Characteristics
The iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens for Daily Wear is available in spherical, multifocal, toric, and toric-multifocal designs. Specifically, the iO2 Sphere, iO2 Toric, ASTERA Multifocal iO2, and ASTERA Multifocal Toric iO2 models are hemispheric flexible shells of the following parameters:
| | iO₂ Sphere | ASTERA<br>Multifocal<br>iO₂ | iO₂ Toric | ASTERA<br>Multifocal<br>Toric iO₂ |
|--------------------------------------|----------------------|----------------------------------------------------|-------------------------------------|----------------------------------------------------|
| Diameter(s) | 10.0 mm to 16.0 mm | | | |
| Center Thickness<br>(Low Minus Lens) | 0.07 mm dry | | | |
| Center Thickness<br>(Plus Lens) | Up to 0.50 mm | | | |
| Base Curve(s) | 6.5 mm - 9.9 mm | | | |
| Powers | -30.00 D to +30.00 D | | | |
| Cylinder Powers | Not Applicable (N/A) | | Up to-10.00 D<br>in steps of 0.25 D | |
| Axis | Not Applicable (N/A) | | 1° to 180° | |
| Add Powers | N/A | P1/ to +1.50<br>P2/ +1.75 to +2.25<br>P3/ +2.50 up | N/A | P1/ to +1.50<br>P2/ +1.75 to +2.25<br>P3/ +2.50 up |
All iO2 lenses are plasma treated in the dry state prior to initial hydration.
----
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The lens material (mangofilcon A) is a non-ionic hydrophilic copolymer that consists of 51% mangofilcon A and 49% water by weight. Mangofilcon A is available clear (no tint) with or without a UV absorber to block a significant amount of the UV radiation occurring between 200 and 400 nm (UVA and UVB). Mangofilcon A is also available in Blue or Aqua visibility tints to assist with handling. Both colors are available with or without the UV absorber.
The.physicochemical properties of iO2 (mangofilcon A) Soft (hydrophilic) Contact Lenses for Daily Wear are tabulated at the top of the next page:
510(k) Summary Page 2 of 5
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Image /page/2/Picture/0 description: The image shows a logo for Alden Optical. The logo consists of a stylized eye-like symbol above the words "ALDEN" and "OPTICAL", which are stacked vertically. The text is in a simple, sans-serif font, and the overall design is clean and professional.
| Characteristic | Value |
|-------------------------------|-------------------------------|
| Dk | 49<br>(Fatt Units @ 35°C) |
| REFRACTIVE INDEX | Dry: 1.470<br>Hydrated: 1.413 |
| SPECIFIC GRAVITY | Dry: 1.112<br>Hydrated: 1.109 |
| LINEAR EXPANSION RATIO | 1.26 |
| WATER CONTENT | 49% |
| LIGHT TRANSMITTANCE | Clear: 96%T<br>Tinted: >70%T |
| PLASMA TREATMENT REQUIRED | Yes |
| SHORE D HARDNESS (blank form) | ≥ 83 |
### iO2 (mangofilcon A) Physicochemical Properties
#### IV. Indications for Use
i
. .
The iO2 Sphere (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of myopia and hyperopia in aphakic or non-aphakic patients with nondiseased eyes who exhibit no more than 2.00 D of astigmatism and can obtain satisfactory visual acuity in a power range of +30.00 to -30.00 D.
The ASTERA Multifocal iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of presbyopia in myopic and hyperopic eyes in aphakic or non-aphakic patients with non-diseased eyes who exhibit no more than 2.00 D of astigmatism and can obtain satisfactory visual acuity in a power range of +30.00 to -30.00 D and have near add requirements up to 3.25 D.
The iO2Toric (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of refractive ametropia (myopia, and astigmatism) in aphakic or non-aphakic persons with non diseased eyes in a spherical power range of +30.00 to
30.00 D and a cylinder power range up to -10.0D.
The ASTERA Multifocal Toric iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of presbyopia in myopic. hyperopic and astigmatic aphakic or non-aphakic patients with non-diseased eyes in a spherical power range of 430.00 to -30.00 D. a cylinder power range up to -10.00 D and an add requirement up to 3.25 D.
iO2 lenses may be disinfected using chemical (not heat) disinfecting systems.
510(k) Summary Page 3 of 5
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Image /page/3/Picture/0 description: The image shows a logo for Alden Optical. The logo features a stylized letter 'A' inside a curved shape, positioned above the words 'ALDEN' and 'OPTICAL', which are stacked vertically. The text is in a bold, sans-serif font, and the overall design is simple and modern.
#### V. Comparison to Legally Marketed Predicate
| PROPERTY | iO2(mangofilcon A)<br>(subject device) | LSH (mangofilcon A)<br>(predicate device) |
|-------------------------|----------------------------------------|-------------------------------------------|
| Marketing Status | Not Yet Cleared | K120756 |
| USAN | Mangofilcon A | Mangofilcon A |
| Device Class | II | II |
| FDA Product Code | LPL | LPL |
| Regulation | 21 CFR 886.5925 | 21 CFR 886.5925 |
| Intended Use | Same as predicate LSH | Same as subject iO2 |
| Manufacturing Method | Lathe-cut | Lathe-cut |
| Plasma Treatment? | Yes | Yes |
| Water Content | 49% | 49% |
| Oxygen Transmissibility | 49 (ISO/Fatt) | 49 (ISO/Fatt) |
| Refractive Index | Dry: 1.470<br>Hydrated: 1.413 | Dry: 1.470<br>Hydrated: 1.413 |
| Specific Gravity | Dry: 1.112<br>Hydrated: 1.109 | Dry: 1.112<br>Hydrated: 1.109 |
| Shore D Hardness | ≥83 | ≥ 83 |
| Tensile Strength | 3.07 M Pa | 3.07 M Pa |
| Elongation at Break | 470% | 470% |
| Light Transmittance | Clear: 96%T<br>Tinted: >70%T | Clear: 96%T<br>Tinted: >70%T |
#### Summary of Non-Clinical Performance Data VI.
* A combination of relevant non-clinical analysis and testing has been assured, including:
-----------------------------------------------------------------------------------
| • Chemical composition of finished lenses | • Color and light transmittance |
|----------------------------------------------------|---------------------------------|
| • Purity of initial monomers | • Refractive index |
| • Shelf Life | • Water content |
| • Leachability of Residual Monomers | • Oxygen transmissibility |
| • Leachability of Color Additives / UV<br>Absorber | • Specific gravity |
| • Biocompatibility testing | • Mechanical Testing & Hardness |
| • Preservative Uptake and Release | • Lens/Solution Compatibility |
510(k) Summary Page 4 of 5
### C-5
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Image /page/4/Picture/0 description: The image shows a logo for Alden Optical. The logo features the words "ALDEN OPTICAL" in a stacked format, with "ALDEN" on top and "OPTICAL" below. Above the text is a stylized graphic element that resembles an eye or a lens shape. The logo is in black and white and has a slightly distressed or vintage appearance.
# VIII. Conclusions Drawn
:
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It is the conviction of Alden Optical Laboratories that the information and data submitted in this premarket notification substantiate our ability to manufacture a contact lens with a safety and effectiveness profile that is substantially equivalent to the predicate device, and that does not raise different questions of safety and effectiveness. ·Based on these facts, Alden therefore concludes that the subject device is as safe and as effective, that is, "substantially equivalent" to, the predicate pursuant to section 513(i) of the Act.
### END OF 510(k) SUMMARY
510(k) Summary Page 5 of 5
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DEPARTMENT OF HEALTH & HUMAN SERVICES
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Public Health Service
February 19, 2014
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
Alden Optical Laboratories. Inc. % Mr. Kevin Randall, RAC ComplianceAcuity, Inc. 16576 W. 53d Way Golden, CO 80403
Re: K133079
Trade Name: iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens for Daily Wear Regulation Number: 21 CFR 886.5925 Regulation Name: Soft (hydrophilic) contact lens Regulatory Class: II Product Code: LPL Dated: November 5, 2013 Received: November 6, 2013
Dear Mr. Randall:
This letter corrects our substantially equivalent letter of December 17, 2013.
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration. Ilsting of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you; however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies.
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You must comply with all the Act's requirements, including, but not limited to: Registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm 1 15809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours.
# Kesia Y. Alexander -S
for Malvina B. Eydelman, M.D. Director Division of Ophthalmic and Ear. Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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## Indications for Use
510(k) Number (if known): K133079
Device Name: iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens for Daily Wear
Indications For Use:
The iO2 Sphere (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of myopia and hyperopia in aphakic or non-aphakic patients with nondiseased eves
who exhibit no more than 2.00 D of astigmatism and can obtain satisfactory visual acuity in a power range of +30.00 to -30.00 D.
The ASTERA Multifocal iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of presbyopia in myopic and hyperopic eyes in aphakic or nonaphakic patients with non-diseased eyes who exhibit no more than 2.00 D of astigmatism and can obtain satisfactory visual acuity in a power range of +30.00 to -30.00 D and have near add requirements up to 3.25 D.
The iO2Toric (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of refractive ametropia (myopia, and astigmatism) in aphakic or non- aphakic persons with non diseased eyes in a spherical power range of +30.00 to -30.00 D and a cylinder power range up to -10.0D.
The ASTERA Multifocal Toric iO2 (mangofilcon A) Soft (hydrophilic) Contact Lens is indicated for the correction of presbyopia in myopic, hyperopic and astigmatic aphakic or non- aphakic patients with non-diseased eyes in a spherical power range of +30.00 to -30.00 D, a cylinder power range up to -10.00 D and an add requirement up to 3.25 D.
iO2 lenses may be disinfected using chemical (not heat) disinfecting systems.
Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Page 1 of _ 2 __
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Concurrence of CDRH, Office of Device Evaluation (ODE)
Joseph C. Hutter -S 2013.12.13 13:18:08 -05'00'
(Division Sign-Off) Division of Ophthalmic and Ear, Nose and Throat Devices
510(k) Number_K133079_
Page 2 of ___2__
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