IONOSIT BOND

K991172 · Dmg Chemisch Pharmazeutische Fabrik GmbH · EMA · May 17, 1999 · Dental

Device Facts

Record IDK991172
Device NameIONOSIT BOND
ApplicantDmg Chemisch Pharmazeutische Fabrik GmbH
Product CodeEMA · Dental
Decision DateMay 17, 1999
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 872.3275
Device ClassClass 2

Indications for Use

Ionosit Bood is indicated for use in lining and basing applications under composite, amalgam ceramic and metal restorations.

Device Story

Ionosit Bond is a light-cure, glass ionomer liner/base material used in dental procedures. It is supplied as a powder and liquid system that requires mixing prior to application. The liquid contains a light-sensitive polymerizable acid, while the powder contains a fluoride-releasing reactive glass. The material is applied by a dental professional under various restorative materials (composite, amalgam, ceramic, metal) to serve as a liner or base. It functions to provide a protective layer beneath the final restoration. No clinical data was provided; safety and effectiveness are established through design and technical equivalence to predicate glass ionomer materials.

Clinical Evidence

No clinical data included. Substantial equivalence based on design and technical specifications.

Technological Characteristics

Light-cure glass ionomer liner/base. Components: powder (fluoride-releasing reactive glass) and liquid (light-sensitive polymerizable acid). Complies with ISO 9917-Part 2 (dental water-based cements).

Indications for Use

Indicated for lining and basing applications under composite, amalgam, ceramic, and metal restorations in dental patients.

Regulatory Classification

Identification

Zinc oxide-eugenol is a device composed of zinc oxide-eugenol intended to serve as a temporary tooth filling or as a base cement to affix a temporary tooth filling, to affix dental devices such as crowns or bridges, or to be applied to a tooth to protect the tooth pulp. Dental cement other than zinc oxide-eugenol is a device composed of various materials other than zinc oxide-eugenol intended to serve as a temporary tooth filling or as a base cement to affix a temporary tooth filling, to affix dental devices such as crowns or bridges, or to be applied to a tooth to protect the tooth pulp.

Predicate Devices

Submission Summary (Full Text)

{0}------------------------------------------------ K991172 Ionosit Bond MAY 17 # 510(k) Summary | Trade Name: | Ionosit Bond | |----------------------|---------------------------------------------------------------------------------------------------------------------| | Sponsor: | DMG Chemisch-Pharmazeutische Fabrik GmbH<br>Elbgaustrasse 248<br>22547 Hamburg, Germany<br>Registration No. 8010567 | | Device Generic Name: | Dental cement | | Classification: | According to Section 513 of the Federal Food, Drug, and<br>Cosmetic Act the device classification is Class II | # Predicate Device: The proposed DMG Ionosit Bond material is substantially equivalent to the Vitrebond material mirketed by 3M Dental Products, which was cleared for marketing by FDA in K962065 and K882821. # Product Description: Ionosit Bourd is a light-cure, glass ionomer liner/base material which is supplied in the form of a powder and liquid that are mixed prior to use. The liquid component contains a light sensitive polymerizable acid; the powder contains a fluoride-releasing special reactive glass. ### Indications for Use: Ionosit Bood is indicated for use in lining and basing applications under composite, amalgam ceramic and metal restorations. # Safety and Performance: Substantial equivalence for this device was based solely on design and technical specifications; no performance or safety data was included in this premarket notification. The materials, performance specifications and essential design characteristics of the Ionosit Bond material are equivalent to those of the predicate device. The proposed Ionosit Bond material conplies with FDA's Guidance for Dental Cements as well as ISO 9917-Part 2 (dental water-based cements). # Conclusion: Based on the indications for use, technological characteristics, and comparison to the predicate device, the Ionosit Bond material has been shown to be safe and effective for its intended use. {1}------------------------------------------------ K991158 : 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上一篇: 上 : | (5) Technological characteristic of the gloves. | | | | | | |-------------------------------------------------|------------------|----------|------------------------------|-----------|---------| | a. Dimensions | | | | | | | Sizes | XS | S | M | L | XL | | Length | 240 mm | 240 mm | 240 mm | 240 mm | 240 mm | | Width | 80 < mm | 80±10 mm | 95±10 mm | 111±10 mm | >111mm | | Thickness | | | | | | | 1. Cuff (min) | 0.10 mm | 0.10 mm | 0.10 mm | 0.10 mm | 0.10 mm | | 2. Palm (min) | 0.10 mm | 0.10 mm | 0.10 mm | 0.10 mm | 0.10 mm | | 3. Finger Tip (min) | 0.10 mm | 0.10 mm | 0.10 mm | 0.10 mm | 0.10 mm | | b. Physical Properties | | | | | | | | Before aging | | After aging at 70°C 168 hrs. | | | | | Tensile Strength | 21 Mpa | | 16 Mpa | | | Ultimate Elongation | 700 % (min.) | | 600 % (min.) | | | (6) Performance data is the same as mentioned immediately above. (7) Clinical date is not needed for gloves or for most devices cleared by the 510 (K) process. - (8) Non-clinical data We certify that these gloves meet ASTM D 3578 Standard. Meets FDA pinhole requirement. Meets labeling claim.
Innolitics

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