Skip to content

KneePlus Knee+

by Pixee Medical 3 variants

KneePlus Knee+ (KNS002) is a Class II device made by Pixee Medical, listed in FDA GUDID since 16 Jun 2023 (UDI-DI 03760297030315), 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 Number03760297030315 UDI-DI Date16 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
KneePlus
Generic name
Orthopaedic stereotactic surgery system
Model / Ref / Catalog
Knee+, KNS002
Primary DI / UDI-DI
03760297030315
FDA product code
OLO
GMDN term
Orthopaedic stereotactic surgery system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic stereotactic surgery system

Similar devices in this category

Other devices filed under Orthopaedic stereotactic surgery system.

Other devices from Pixee Medical

See all devices from Pixee Medical →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)