XANTOPREN COMFORT

K991425 · Heraeus Kulzer, Inc. · ELW · Jun 15, 1999 · Dental

Device Facts

Record IDK991425
Device NameXANTOPREN COMFORT
ApplicantHeraeus Kulzer, Inc.
Product CodeELW · Dental
Decision DateJun 15, 1999
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 872.3660
Device ClassClass 2

Indications for Use

Xantopren Comfort is a silicone based condensation curing impression material used for all inlay, crown and bridge, edentulous and partial impressions. The Xantopren Comfort Activator is the catalyst. This product is packaged in a cartridge delivery system which will dispense equal amounts of base and activator.

Device Story

Xantopren Comfort is a silicone-based, condensation-curing dental impression material. It consists of a base paste and an activator catalyst. The device utilizes a cartridge delivery system to ensure precise, homogenous mixing of base and catalyst through a mixing tip, preventing user manipulation of material properties. Dentists use the material in clinical settings to create impressions for inlays, crowns, bridges, and partial or edentulous cases. The material is applied to impression trays; it flows around tooth preparations and into the sulcus. The cartridge system features adjustable injection tips for ease of application. The resulting impressions are compatible with standard condensation or addition silicone products for pouring. The device benefits the patient by providing high-quality, accurate dental impressions for restorative procedures.

Clinical Evidence

Clinical handling evaluation performed on a minimum of 20 impressions. Metrics included dispensing ease, viscosity, working/setting times, color differentiation, impression quality, and disinfection ease. Results indicated excellent color differentiation, very good impression quality, and adequate working/setting times consistent with comparable materials. No distortion observed after disinfection. Bench testing compared physical properties (Shore A hardness, deformation, recovery, linear dimensional change) against predicate devices, showing similar performance profiles.

Technological Characteristics

Condensation-curing silicone impression material. Supplied in a cartridge delivery system for automated, homogenous mixing. Physical properties include Shore A hardness (36-38), recovery from deformation (>98%), and linear dimensional change (1.0%). Compatible with standard condensation and addition silicone pouring materials. No electronic components or software.

Indications for Use

Indicated for dental impressions including inlay, crown and bridge, edentulous, and partial impressions.

Regulatory Classification

Identification

Impression material is a device composed of materials such as alginate or polysulfide intended to be placed on a preformed impression tray and used to reproduce the structure of a patient's teeth and gums. The device is intended to provide models for study and for production of restorative prosthetic devices, such as gold inlays and dentures.

Special Controls

*Classification.* Class II (Special Controls).

Predicate Devices

Submission Summary (Full Text)

{0}------------------------------------------------ K991425 JUN 1 5 1999 # 510(K) Summary June 7, 1999 Date: Heraeus Kulzer, Inc. Address: 4315 S. Lafayette Blvd. South Bend, IN. - Cheryl V. Zimmerman Contact: 219-299-6662 - Xantopren Comfort Base Device: Xantopren Activator ### Substantially Equivalent to: CutterSil Light [K760756] KAI0165 CutterSil Mucosa CutterSil Universal Hardener (Paste & Liquid) [K760756] ### Device Description: Xantopren Comfort is a is silicone based condensation curing impression material used for all inlay, crown and bridge, edentulous and partial impressions. The advantage of Xantopren Comfort Light and Xantopren Comfort Medium is that the product is available in a cartridge delivery system that ensures that the correct amount of base and catalyst is used each time. With the cartridge delivery system a homogenous mix is obtained each time the material is expressed through the mixing tip. The user cannot manipulate the properties of the product because of the delivery system. An evaluation of the clinical handling characteristics was evaluated for: - dispensing of material(s) ● - viscosity for application . - working time . - setting time - color differentiation e - quality of impression . - ease of disinfection. . The putty material was used in conjunction with the low viscosity and the medium viscosity Xantopren. A minimum of 20 impressions were taken. Dispensing of the putty material is easily accomplished. One measuring scoop provides adequate material for either a bite or quadrant impression tray. Two measuring scoops are sufficient for a full {1}------------------------------------------------ arch impression tray. After bleeding the cartridge, the low and medium Xantopren visciosities flowed well and were easily extruded through the mixing tip with no difficulty. The low and medium viscosity Xantopren were determined to be quite good for impressions. Both viscoisties flow well around the tooth preparation and into the sulcus. The working time and setting time was determined to be adequate, within the ranges stated in the instructions and similar to comparable impression materials. Color differentiation between the low and medium viscosities and the putty's received an excellent rating. The quality of the impression is very good. And both Xantopren Light and Medium bond well to currently marketed products CutterSil Putty Plus and CutterSil Comfort. The injection tips on the cartridge delivery system can be angled to suit the needs to the dentist. Pouring of the impression is compatible with silicone products (condensation or addition) that are currently in the market place. Ease of disinfection is consistent with similar materials, and no distortion was observed after disinfection. | PROPERTIES | Xantopren Comfort Light | CutterSil Light | |-------------------------------------|-------------------------|-----------------| | Mixing Time (s) | - | 30 | | Working Time (min) | 2:00 | 2:00 | | Setting Time (min) | 3:00 | 4:00 | | Shore A Hardness | 36 | - | | Max. Deformation Under Pressure (%) | 8.0 | 2-10 | | Recovery From Deformation (%) | >98 | 97.5 | | Linear Dimensional Change (%) | 1.0 | -1.0 - 0 | | | | | ## Product Comparison: | PROPERTIES | Xantopren Comfort Medium | CutterSil Medium | |---------------------------------|--------------------------|------------------| | Mixing Time | - | 45 | | Working Time | 2:30 | 2:00 | | Setting Time | 3:30 | 4:00 | | Shore A Hardness | 38 | - | | Max. Deformation Under Pressure | 7.5 | 2-10% | | Recovery From Deformation | >98 | 97.5 | | Linear Dimensional Change | 1.0 | -1.0 -0 | {2}------------------------------------------------ Image /page/2/Picture/1 description: The image is a black and white seal for the Department of Health & Human Services - USA. The seal is circular with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter of the circle. Inside the circle is a stylized image of an eagle. Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 JUN 1 5 1999 Ms. Cheryl V. Zimmerman Quality Operations and Regulatory Affairs Heraeus Kulzer, Incorporated 4315 South Lafayette Boulevard South Bend, Indiana 46614-2517 Re: K991425 Xantopen® Comfort Trade Name: Requlatory Class: II Product Code: ELW Dated: April 21, 1999 Received: April 23, 1999 Dear Ms. Zimmerman: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act of the Act. include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may Existing major be subject to such additional controls. requlations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) requlation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP requlation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Reqister. {3}------------------------------------------------ Page 2 - Ms. Zimmerman this response to your premarket notification Please note: submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling requlation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4692. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html". Sincerely yours Timothy A. Ulatowski Director Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ Page 1 of 1 # 510(k) Number (if Known): Device Name: Xantropren Comfort Base Paste and Activator Indications For Use: Xantropren Comfort is a silicone based condensation curing impression material used for all inlay, crown and bridge, edentulous and partial impressions. The Xantropren Comfort Activator is the catalyst. This product is packaged in a cartridge delivery system which will dispense equal amounts of base and activator. (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device evaluation (ODE) | Prescription Use<br>(Per 21 CFR 801.109) | <div style="display:inline-block; vertical-align:middle;">✓</div> | OR | Over-The-Counter Use | | |------------------------------------------------------------------------|-------------------------------------------------------------------|--------------------------|----------------------|--| | <hr/> | | | | | | | Susan Runver | (Optional Format 1-2-96) | | | | (Division Sign-Off) | | | | | | Division of Dental, Infection Control,<br>and General Hospital Devices | | | | | | 510(k) Number | 1911925 | | | |
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