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Apixia 10811

by Dentamerica

Apixia 10811 is a Class I device made by Dentamerica, listed in FDA GUDID since 22 Apr 2026 (UDI-DI 00850461008202), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850461008202 UDI-DI Date22 Apr 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  • Withdrawn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
Apixia
Generic name
Dental x-ray film holder, single-use
Model / reference
10811
Primary DI / UDI-DI
00850461008202
FDA product code
EGZ
GMDN term
Dental x-ray film holder, single-use
Device class
Class I
Regulation number
872.1905
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EGZ (Holder, Film, X-Ray).

Other devices from Dentamerica

See all devices from Dentamerica →

Properties

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