FDA Device Intelligence
Home › KENEX (ELECTRO-MEDICAL) LIMITED › KENEX

KENEX

KENEX (ELECTRO-MEDICAL) LIMITED · Model 1350/1 · UDI-DI 05055449415989

IXA Prescription
10
510(k) clearances
11
Adverse events
1
Recalls
16
Facilities

Description

1350/1 Mobile Tube Head with Detector Holder

Recalls

DateFirmReason
2005-01-26AGFA Corp.Users of these cassettes may detect poor film to screen contact and unsatisfactory sharpness of radiographic images.

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.