9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WaveLight FS200 Patient Interface
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306822599·Bow Retractors without teeth, Width: 35 mm / 1....
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
PSM LOMAS / BENEFIT SCREWS
FDA 510(k)
FDA Class 2
·Dental
SYNERGY
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·July 25, 2011
GYNECARE TVT OBURATOR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·June 26, 2013
3856LF TED STKG NYL T/L LL
FDA Adverse Event
Malfunction
·COSTA RICA·Product code FQL·October 21, 2014
BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026
Exactech Equinoxe REVERSE SHOULDER,36mm Humeral Liner: a) +0mm, Item Number 320-36-00, b) +2.5mm, Item Number 320-36-03; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024