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KneeKG system 0

by Emovi Inc

KneeKG system 0 (P-142) is a Class II device made by Emovi Inc, cleared under FDA 510(k) K091000 on 26 Oct 2009 and listed in FDA GUDID since 23 Mar 2022 (UDI-DI 00627843933236), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K091000

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00627843933236 UDI-DI Date23 Mar 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) from GUDID NumberK091000 Date26 Oct 2009IssuedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K091000 decided 26 Oct 2009 Active
  • FDA GUDID UDI-DI 00627843933236 listed 23 Mar 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K091000
  2. Listed FDA GUDID 00627843933236

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
KneeKG system
Generic name
Gait analysis system
Model / Ref / Catalog
0, P-142
Primary DI / UDI-DI
00627843933236
510(k) Number
FDA product code
LXJ
GMDN term
Gait analysis system
Device class
Class II
Regulation number
890.5360
GUDID distribution status
In Commercial Distribution

Related devices

Category: Gait analysis system

Similar devices

Other devices filed under FDA product code LXJ (Interactive Rehabilitation Exercise Devices).

Other devices from Emovi Inc

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)