Identity
- Trade Name
- DIRECTCROWN FDA UDI
- Generic Name
- Dental bridge, polymer FDA UDI
- Device Name
- 2-SMALL POSTERIOR UPPER RIGHT MOLAR REFILL PACKAGE OF THREE (3) NATURAL 1 CROWNS FDA UDI
- Model / Reference
- NAT2S FDA UDI
- Description
- 2-SMALL POSTERIOR UPPER RIGHT MOLAR REFILL PACKAGE OF THREE (3) NATURAL 1 CROWNS FDA UDI
Identifiers
- Primary DI / UDI-DI
- D752NAT2S1 FDA UDI
- FDA Product Code
- EBG FDA UDI
- GMDN Term
- Dental bridge, polymer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3770 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental bridge, polymer
Directcrown by Direct Crown Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Direct Crown Products
Sources (1)
- FDA UDI 00de724c-535d-4b87-8b7c-88a73324bcd6 34 fields · synced May 30, 2026