Preci-Clix 0101274
Preci-Clix 0101274 is a Class I device made by PREAT Corporation, listed in FDA GUDID since 28 Jun 2022 (UDI-DI 00842092127223), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00842092127223 | Date28 Jun 2022 | StatusListed |
Official records
- AccessGUDID record 00842092127223
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Preci-Clix
- Generic name
- Overdenture
- Model / Ref / Catalog
- 0101274
- Primary DI / UDI-DI
- 00842092127223
- FDA product code
- EGG
- GMDN term
- Overdenture
- Device class
- Class I
- Regulation number
- 872.3165
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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