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Abiding Mu Scanbody Amsb

by SNUCONE Co., LTD.

Abiding Mu Scanbody Amsb is a Class I device made by SNUCONE Co., LTD., listed in FDA GUDID since 22 May 2026 (UDI-DI 08800020856661), 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 Number08800020856661 UDI-DI Date22 May 2026ListedStatusListed 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  • Withdrawn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
Abiding Mu Scanbody
Generic name
Dental implant abutment analog, intraoral-scanning, single-use
Model / reference
AMSB
Primary DI / UDI-DI
08800020856661
FDA product code
NDP
GMDN term
Dental implant abutment analog, intraoral-scanning, single-use
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from SNUCONE Co., LTD.

See all devices from SNUCONE Co., LTD. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (8, all answered No)