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Princeton 45110-02

by Princeton Medical Group, Inc.

Princeton 45110-02 is a Class I device made by Princeton Medical Group, Inc., listed in FDA GUDID since 18 Sep 2025 (UDI-DI 00810158217119), 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 Number00810158217119 UDI-DI Date18 Sep 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  • Withdrawn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
General-purpose curette
Model / reference
45110-02
Primary DI / UDI-DI
00810158217119
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
  • Lot / batch number
Other properties (12, all answered No)