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Apoza Cam-II

by Apoza Enterprise Co., Ltd.

Apoza Cam-II is a Class I device made by Apoza Enterprise Co., Ltd., listed in FDA GUDID since 28 Jun 2023 (UDI-DI 04719883751423), 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 Number04719883751423 UDI-DI Date28 Jun 2023ListedStatusListed 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  • Withdrawn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
Apoza
Generic name
Intraoral camera
Model / reference
CAM-II
Primary DI / UDI-DI
04719883751423
FDA product code
NRD
GMDN term
Intraoral camera
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Intraoral camera

Other devices from Apoza Enterprise Co., Ltd.

See all devices from Apoza Enterprise Co., Ltd. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)