8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SECURE-ALL 1-PIECE BODY HOLDER, SMALL/MEDIUM (24451-010,020,24452-010,020,030)
FDA 510(k)
FDA Class 1
·General Hospital
MediClear PreOp
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PERIPATCH ENDO-SLEEVE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
21 REC CANISTER
FDA Adverse Event
Malfunction
·AMSINO MEDICAL CO., LTD.·Product code GCX·April 10, 2014
ADVANTA VXT
FDA Adverse Event
Injury
·ATRIUM MEDICAL CORP.·Product code DSY·January 2, 2013
8800
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·December 20, 2010
1.85MM TI MATRIX SCREW SELF-TAPPING/4MM
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code JEY·January 21, 2015
CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026