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Skytron

SKYTRON LLC · Model 1-011-06-33 · UDI-DI 10841736117641

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

Description

LEG SECTION 3501B, 3501C, 3502, 3503, 3600 SERIES, GS70 3 Inch SOF PAD WELDED SEAMS

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

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.