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Guide System Starter Set, PL J5300.0074

by ALTATEC GmbH 2 variants

Guide System Starter Set, PL J5300.0074 is a Class I device made by ALTATEC GmbH, listed in FDA GUDID since 17 Aug 2026 (UDI-DI 04099797012675), 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 Number04099797012675 UDI-DI Date17 Aug 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  • Withdrawn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
Guide System Starter Set, PL
Generic name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
J5300.0074
Primary DI / UDI-DI
04099797012675
FDA product code
EJL
GMDN term
Dental/maxillofacial surgical procedure kit, non-medicated, reusable
Device class
Class I
Regulation number
872.3240
GUDID distribution status
In Commercial Distribution

Other devices from ALTATEC GmbH

See all devices from ALTATEC GmbH →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)