Identity
- Trade Name
- Mollosil Plus Full Kit FDA UDI
- Generic Name
- Denture reliner, elastic, short-term FDA UDI
- Device Name
- Mollosil Plus Full Kit - Mollosil plus cartridge, glaze and catalyst and adhesion promoter FDA UDI
- Model / Reference
- FIXX1 FDA UDI
- Description
- Mollosil Plus Full Kit - Mollosil plus cartridge, glaze and catalyst and adhesion promoter FDA UDI
Identifiers
- Primary DI / UDI-DI
- D814FIXX11 FDA UDI
- FDA Product Code
- EBI FDA UDI
- GMDN Term
- Denture reliner, elastic, short-term FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3760 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Denture reliner, elastic, short-term
Mollosil Plus Full Kit by Protech Professional Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Denture reliner, elastic, short-term.
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- COE-COMFORT™ — Gc America Inc. · Class II
- COE-COMFORT™ — Gc America Inc. · Class II
- GC Reline ™ — Gc America Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Protech Professional Products, Inc.
Sources (1)
- FDA UDI 9c0a1199-5a84-4b3c-b8bf-7e9edef7f58e 33 fields · synced May 30, 2026