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OSSEOUS-SnorOFF E31701

by Eon Meditech Private Limited

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08904461055031 UDI-DI Date13 Mar 2026ListedStatusListed 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  • Withdrawn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
OSSEOUS-SnorOFF
Generic Name
Sleep-disordered breathing tongue electrical stimulator
Model / Reference
E31701
Primary DI / UDI-DI
08904461055031
FDA Product Code
BYP
GMDN Term
Sleep-disordered breathing tongue electrical stimulator
Device Class
Class I
Regulation Number
868.5620
GUDID distribution status
In Commercial Distribution

Other devices from Eon Meditech Private Limited

See all devices from Eon Meditech Private Limited →

Properties

  • Sterile
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No