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Princeton 75128-03

by Princeton Medical Group, Inc.

Princeton 75128-03 is a Class I device made by Princeton Medical Group, Inc., listed in FDA GUDID since 8 Mar 2024 (UDI-DI 00810158210806), 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 Number00810158210806 UDI-DI Date8 Mar 2024ListedStatusListed 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  • Withdrawn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
General-purpose curette
Model / reference
75128-03
Primary DI / UDI-DI
00810158210806
FDA product code
FZS
GMDN term
General-purpose curette
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: General-purpose curette

Other devices from Princeton Medical Group, Inc.

See all devices from Princeton Medical Group, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)