Identity
- Trade Name
- VersaLite FDA UDI
- Generic Name
- Dental composite resin FDA UDI
- Device Name
- VersaLite A1 prefilled tips, 20 FDA UDI
- Model / Reference
- 330600 FDA UDI
- Description
- VersaLite A1 prefilled tips, 20 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817051020983 FDA UDI
- 510(k) Number
- K823510 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
VersaLite by Centrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
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- 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
K823510 also covers:
- VersaLite — CENTRIX, INC.
- VersaLite — CENTRIX, INC.
- VersaLite — CENTRIX, INC.
- VersaLite — CENTRIX, INC.
- VersaLite — CENTRIX, INC.
- Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC
- MASTER-DENT — DENTONICS, INC.
- MASTER-DENT — DENTONICS, INC.
- MASTER-DENT — DENTONICS, INC.
- MASTER-DENT — DENTONICS, INC.
- Henry Schein — HENRY SCHEIN, INC.
- SciPharm Anterior/Posterior Restoratives — SCIENTIFIC PHARMACEUTICALS, INC.
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
- Centrix, Inc.
Sources (1)
- FDA UDI 76bd5423-191e-4c5b-9d95-b207f632f88c 34 fields · synced Jun 6, 2026