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Verasense

by Orthosensor Inc 104 variants

Listed FDA GUDID listing, not in commercial distribution

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 8 Jun 2026. What this means

Regulatory status

as of registry sync 8 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816818021249 UDI-DI Date2 Jun 2017ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Arthroplasty force sensor
Model / Ref / Catalog
VERASENSE for Smith & Nephew Legion PS size 7-8, SNN-LGNPS78
Primary DI / UDI-DI
00816818021249
FDA Product Code
ONN
GMDN Term
Arthroplasty force sensor
Device Class
Class II
Regulation Number
882.4560
GUDID distribution status
Not in Commercial Distribution

Other devices from Orthosensor Inc

See all devices from Orthosensor Inc →

Properties

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

Other properties (7)

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