FDA Device Intelligence
Home › Orfit Industries NV › Orfit Industries

Orfit Industries

Orfit Industries NV · Model 32005/10-V2 · UDI-DI 05420028754122

LWG
4
510(k) clearances
36
Adverse events
1
Recalls
59
Facilities

Description

Leg Support

Recalls

DateFirmReason
2016-04-19Berchtold Corp.The Surgical Table Cushion (HybriGel Pads) could potentially contain staples that's secure two underlying fabrics, which would be captured on certain scans on patients, such as x-r

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.