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American Medicals 1

by American Medicals 1,000+ variants

American Medicals 1 is a Class I device made by American Medicals, listed in FDA GUDID since 20 May 2026 (UDI-DI B35675440110), 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 NumberB35675440110 UDI-DI Date20 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
American Medicals
Generic name
Periosteal elevator, single-use
Model / reference
1
Primary DI / UDI-DI
B35675440110
FDA product code
HTE
GMDN term
Periosteal elevator, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Microwave Radiation

Other devices from American Medicals

See all devices from American Medicals →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)