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J & J Instruments 01-210

by J&J Instruments, LLC

J & J Instruments 01-210 is a Class I device made by J&J Instruments, LLC, listed in FDA GUDID since 29 May 2018 (UDI-DI 00817524020113), 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 Number00817524020113 UDI-DI Date29 May 2018ListedStatusListed 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  • Withdrawn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
Endodontic plugger
Model / Ref / Catalog
01-210
Primary DI / UDI-DI
00817524020113
FDA product code
EKR
GMDN term
Endodontic plugger
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 6.75 Inch

Related devices

Category: Endodontic plugger

Similar devices

Other devices filed under FDA product code EKR (Plugger, Root Canal, Endodontic).

Other devices from J&J Instruments, LLC

See all devices from J&J Instruments, LLC →

Properties

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