FDA Device Intelligence
HomeDevice types › IXA

Cassette, Radiographic Film

FDA product code IXA · Class 2 · Radiology

222
Registered devices
11
Adverse events
1
Recalls
51
510(k) clearances

Devices with this code

Recent 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
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.