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Zekrya Small Arc 003-61097

by DMG America LLC

Zekrya Small Arc 003-61097 is a Class I device made by DMG America LLC, listed in FDA GUDID since 12 Dec 2022 (UDI-DI D033003610971), 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 NumberD033003610971 UDI-DI Date12 Dec 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  • Withdrawn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
Zekrya Small Arc
Generic name
Gingival retraction kit
Model / Ref / Catalog
003-61097
Primary DI / UDI-DI
D033003610971
FDA product code
BRW
GMDN term
Gingival retraction kit
Device class
Class I
Regulation number
868.5820
GUDID distribution status
In Commercial Distribution

Other devices from DMG America LLC

See all devices from DMG America LLC →

Properties

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