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Angel Aligner EAB II

by Wuxi EA Medical Instruments Technologies Limited. 6 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06956748700198 UDI-DI Date6 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  • Withdrawn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
Angel Aligner
Generic Name
Orthodontic progressive aligner
Model / Reference
EAB II
Primary DI / UDI-DI
06956748700198
FDA Product Code
NXC
GMDN Term
Orthodontic progressive aligner
Device Class
Class II
Regulation Number
872.5470
GUDID distribution status
In Commercial Distribution

Other devices from Wuxi EA Medical Instruments Technologies Limited.

See all devices from Wuxi EA Medical Instruments Technologies Limited. →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No