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Aseptico Technique AMA-09A2

by Aseptico, Inc.

Aseptico Technique AMA-09A2 is a Class I device made by Aseptico, Inc., listed in FDA GUDID since 6 Dec 2022 (UDI-DI 10817417021811), 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 Number10817417021811 UDI-DI Date6 Dec 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  • Withdrawn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
Aseptico Technique
Generic name
Orthodontic wire
Model / reference
AMA-09A2
Primary DI / UDI-DI
10817417021811
FDA product code
DZC
GMDN term
Orthodontic wire
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic wire

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Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)