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ASSI.ATK1432602

by Accurate Surgical & Scientific Instruments Corp.

ASSI.ATK1432602 is a Class I device made by Accurate Surgical & Scientific Instruments Corp., listed in FDA GUDID since 24 Jun 2020 (UDI-DI 00841645129929), 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 Number00841645129929 UDI-DI Date24 Jun 2020ListedStatusListed 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  • Withdrawn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
Assi
Generic name
Orthopaedic osteotome
Model / reference
ASSI.ATK1432602
Description
Lambotte Ostetomme 17cm, 2mm
Primary DI / UDI-DI
00841645129929
FDA product code
HNR
GMDN term
Orthopaedic osteotome
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic osteotome

Other devices from Accurate Surgical & Scientific Instruments Corp.

See all devices from Accurate Surgical & Scientific Instruments Corp. →

Properties

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