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Surgical Knee Immobilizer KS-9930

by Kapp Surgical Instrument, Inc.

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 NumberB033KS99300 UDI-DI Date12 Aug 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  • Withdrawn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
Surgical Knee Immobilizer
Generic Name
Limb/torso/head restraint, single-use
Model / Reference
KS-9930
Primary DI / UDI-DI
B033KS99300
FDA Product Code
ITQ
GMDN Term
Limb/torso/head restraint, single-use
Device Class
Class I
Regulation Number
890.3475
GUDID distribution status
In Commercial Distribution

Other devices from Kapp Surgical Instrument, Inc.

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Properties

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

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No