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Rinn® 559902

by Dentsply International

Rinn® 559902 is a Class I device made by Dentsply International, listed in FDA GUDID since 24 Nov 2022 (UDI-DI D0035599021), 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 NumberD0035599021 UDI-DI Date24 Nov 2022ListedStatusListed 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  • Withdrawn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
Rinn®
Generic name
Dental x-ray film holder, reusable
Model / Ref / Catalog
559902
Primary DI / UDI-DI
D0035599021
FDA product code
EGZ
GMDN term
Dental x-ray film holder, reusable
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 Dentsply International

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Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)