FDA Device Intelligence
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Glide

INFINITE BIOMEDICAL TECHNOLOGIES, LLC · Model 91000-GL-G · UDI-DI 00850004850671

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

Description

For the Steeper Espire Classic Plus elbow configurations

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.

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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.