Identity
- Trade Name
- Universal Precision Composite Instrument Series FDA UDI
- Generic Name
- Dental material application tool, reusable FDA UDI
- Device Name
- Dental restorative material applicator FDA UDI
- Model / Reference
- 062910 FDA UDI
- Description
- Dental restorative material applicator FDA UDI
Identifiers
- Catalog Number
- 062910 FDA UDI
- Primary DI / UDI-DI
- 07540172012843 FDA UDI
- FDA Product Code
- DZN FDA UDI
- GMDN Term
- Dental material application tool, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Universal Precision Composite Instrument Series by Clinician's Choice Dental Products, Inc. — Class I — FDA UDI — listed in FDA GUDID
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 I | Pending data |
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Manufacturer
- Manufacturer
- Clinician's Choice Dental Products, Inc.
Sources (1)
- FDA UDI 9953e150-135f-4c12-adcf-bf31a7ff9b7f 36 fields · synced May 30, 2026