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Princeton 11140-13

by Princeton Medical Group, Inc.

Princeton 11140-13 is a Class I device made by Princeton Medical Group, Inc., listed in FDA GUDID since 1 Apr 2025 (UDI-DI 00810158214743), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810158214743 UDI-DI Date1 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Princeton
Generic name
ENT soft-tissue cutting forceps
Model / reference
11140-13
Primary DI / UDI-DI
00810158214743
FDA product code
HTD
GMDN term
ENT soft-tissue cutting forceps
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: ENT soft-tissue cutting forceps

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Other devices filed under ENT soft-tissue cutting forceps.

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)