Pomee 705-535
Pomee 705-535 is a Class I device made by Pomee Corporation, listed in FDA GUDID since 7 Dec 2021 (UDI-DI G1577055350), registry data as of 23 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 | NumberG1577055350 | Date7 Dec 2021 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pomee
- Generic name
- Tooth extraction forceps
- Model / Ref / Catalog
- 705-535
- Description
- Extracting Forceps # 53R upper 1st & 2nd molar bayonet right
- Primary DI / UDI-DI
- G1577055350
- FDA product code
- EMH
- GMDN term
- Tooth extraction forceps
- Device class
- Class I
- Regulation number
- 872.4565
- GUDID distribution status
- In Commercial Distribution
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