Identity
- Trade Name
- Renamel® Bulkfill FDA UDI
- Generic Name
- Dental composite resin FDA UDI
- Device Name
- Renamel® Bulkfill A3, 20 Compules FDA UDI
- Model / Reference
- 6722A3 FDA UDI
- Description
- Renamel® Bulkfill A3, 20 Compules FDA UDI
Identifiers
- Catalog Number
- 6722A3 FDA UDI
- Primary DI / UDI-DI
- EDEL6722A31 FDA UDI
- 510(k) Number
- K211259 FDA UDI
- FDA Product Code
- EBF FDA UDI
- GMDN Term
- Dental composite resin FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3690 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
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
Yes
FDA UDI
Category: Dental composite resin
Renamel® Bulkfill by DeltaMed GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental composite resin.
- Name: Light Curing Composite Model: Flow — Micerium S.p.A. · Class IIa
- Forma S — ULTRADENT PRODUCTS, INC. · Class II
- NovaPro Fill — NANOVA BIOMATERIALS INC · Class II
- SimpliShade — KERR CORPORATION · Class II
- Bright Flow Core DC 5ml Dentine — DMP Dental Industry S.A. · Class IIa
- Llis — Dentscare Ltda · Class II
- Capo Universal, 6 g — Schütz Dental GmbH · Class II
- OMNICHROMA — TOKUYAMA DENTAL CORPORATION · Class II
Cleared under the same submission
K211259 also covers:
- BulkFill — Cosmedent, Inc.
- Bulkfill — Cosmedent, Inc.
- Bulkfill — Cosmedent, Inc.
- Bulkfill — Cosmedent, Inc.
- Bulkfill — Cosmedent, Inc.
- Bulkfill — Cosmedent, Inc.
- Bulkfill — Cosmedent, Inc.
- Bulkfill — Cosmedent, Inc.
- Bulkfill — Cosmedent, Inc.
- Renamel® Bulkfill — DeltaMed GmbH
- Renamel® Bulkfill — DeltaMed GmbH
- Renamel® Bulkfill — DeltaMed GmbH
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- DeltaMed GmbH
Sources (1)
- FDA UDI 72eacb33-46ff-4a21-8447-929d37848b32 36 fields · synced May 30, 2026