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Pomee 705-001

by Pomee Corporation

Pomee 705-001 is a Class I device made by Pomee Corporation, listed in FDA GUDID since 7 Dec 2021 (UDI-DI G1577050010), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG1577050010 UDI-DI Date7 Dec 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pomee
Generic name
Tooth extraction forceps
Model / Ref / Catalog
705-001
Primary DI / UDI-DI
G1577050010
FDA product code
EMH
GMDN term
Tooth extraction forceps
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tooth extraction forceps

Similar devices

Other devices filed under FDA product code EMH (Forceps, Rongeur, Surgical).

Other devices from Pomee Corporation

See all devices from Pomee Corporation →

Properties

  • Supplied sterile
  • Sterilise before use
  • Premarket exempt
Other properties (12, all answered No)