Home › SKYTRON LLC › Skytron
Skytron
SKYTRON LLC · Model 1-011-06-2C · UDI-DI 10841736117566
4
510(k) clearances
45
Adverse events
1
Recalls
59
Facilities
Description
2 Inch 3PC PAD SET: 3501B 3600B 3501C 3602 3501 CUSTOM VELCRO
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-04-19 | Berchtold 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 docsData 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.
