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Aimgen Max KMDA351555H

by Achimhai Medical Corporation

Aimgen Max KMDA351555H (MDA-351555H-PA) is a Class I device made by Achimhai Medical Corporation, listed in FDA GUDID since 5 Jul 2022 (UDI-DI 08800024957692), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800024957692 UDI-DI Date5 Jul 2022ListedStatusListed 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  • Withdrawn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
Aimgen Max
Generic name
Fixture/appliance dental drill bit, reusable
Model / Ref / Catalog
KMDA351555H, MDA-351555H-PA
Primary DI / UDI-DI
08800024957692
FDA product code
NDP
GMDN term
Fixture/appliance dental drill bit, reusable
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Fixture/appliance dental drill bit, reusable

Other devices from Achimhai Medical Corporation

See all devices from Achimhai Medical Corporation →

Properties

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