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Si-Sq 30210000

by W&H Dentalwerk Burmoos

Si-Sq 30210000 is a medical device (FDA Class I; FDA product code EFB, Handpiece, Air-Powered, Dental) made by W&H Dentalwerk Burmoos, listed in FDA GUDID since 23 Jan 2019 (UDI-DI J021302100001), 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 NumberJ021302100001 UDI-DI Date23 Jan 2019ListedStatusListed 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  • Withdrawn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
Si-Sq
Generic name
Dental implant stability resonance frequency analysis unit
Model / reference
30210000
Primary DI / UDI-DI
J021302100001
FDA product code
EFB
GMDN term
Dental implant stability resonance frequency analysis unit
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental implant stability resonance frequency analysis unit

Other devices from W&H Dentalwerk Burmoos

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)