Skip to content

American Eagle Instruments NYU1

by American Eagle Instruments

American Eagle Instruments NYU1 is a Class I device made by American Eagle Instruments, listed in FDA GUDID since 30 Jun 2026 (UDI-DI 00841013116377), 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 Number00841013116377 UDI-DI Date30 Jun 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  • Withdrawn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
American Eagle Instruments
Generic name
Periodontal hoe
Model / reference
NYU1
Primary DI / UDI-DI
00841013116377
FDA product code
EMQ
GMDN term
Periodontal hoe
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Other devices from American Eagle Instruments

See all devices from American Eagle Instruments →

Properties

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