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Princeton 75111-10

by Princeton Medical Group, Inc.

Princeton 75111-10 is a Class I device made by Princeton Medical Group, Inc., listed in FDA GUDID since 10 Apr 2024 (UDI-DI 00810158211698), 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 Number00810158211698 UDI-DI Date10 Apr 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  • Withdrawn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
Bone hook
Model / reference
75111-10
Primary DI / UDI-DI
00810158211698
FDA product code
GDG
GMDN term
Bone hook
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone hook

Similar devices in this category

Other devices filed under Bone hook.

Other devices from Princeton Medical Group, Inc.

See all devices from Princeton Medical Group, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)