FDA Device Intelligence
HomeBIONIT LABS SRL › Adam's Hand

Adam's Hand

BIONIT LABS SRL · Model AH02-RM1-W1-01 · UDI-DI 08057971592647

IQZ Prescription
0
510(k) clearances
15
Adverse events (1 deaths)
2
Recalls
37
Facilities

Description

Adam's Hand - Right, Medium, White, QDW (device)

Recalls

DateFirmReason
2024-08-22Kinova IncPotential installation issue that could result in a fire hazard in the event of an interaction between a damaged Jaco arm and a wheelchair exhibiting electrical leakage.
2005-02-01Motion Control, Inc.Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard.

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 docs
Data 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.