Home › BIONESS INC. › L300 Go System, Left Small Lower Leg
L300 Go System, Left Small Lower Leg
BIONESS INC. · Model LG4-5V00 · UDI-DI 00815962020146
1
510(k) clearances
50
Adverse events (1 deaths)
2
Recalls
40
Facilities
Description
L300 Go system with Small Left cuff
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-07-19 | Myolyn Inc. | Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock. |
| 2008-08-06 | Innovative Neurotronics, Inc. | Knob responsible for regulating the amount of stimulation administered by the WalkAide System control unit may fall off while device is in use. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.