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Med Atlantic KN-70/XL

by Tianjin Tairuibosi Medical Appliance Co., Ltd.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06974870090253 UDI-DI Date13 Jan 2023ListedStatusListed 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  • Withdrawn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
Med Atlantic
Generic Name
Knee support orthosis
Model / Reference
KN-70/XL
Primary DI / UDI-DI
06974870090253
FDA Product Code
IQI
GMDN Term
Knee support orthosis
Device Class
Class I
Regulation Number
890.3475
GUDID distribution status
In Commercial Distribution

Related devices

Category: Knee support orthosis

Other devices from Tianjin Tairuibosi Medical Appliance Co., Ltd.

See all devices from Tianjin Tairuibosi Medical Appliance Co., Ltd. →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No