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J&J Instruments 04-971

by J&J Instruments, LLC

J&J Instruments 04-971 is a Class I device made by J&J Instruments, LLC, listed in FDA GUDID since 1 Oct 2019 (UDI-DI 00817524022070), 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 Number00817524022070 UDI-DI Date1 Oct 2019ListedStatusListed 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  • Withdrawn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
J&J Instruments
Generic name
Periosteal elevator, reusable
Model / reference
04-971
Primary DI / UDI-DI
00817524022070
FDA product code
EMJ
GMDN term
Periosteal elevator, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Periosteal elevator, reusable

Other devices from J&J Instruments, LLC

See all devices from J&J Instruments, LLC →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)