11 results
·
27ms
·
Sources: EU EUDAMED, US FDA
THORACIC CLAMPS: SAROT, KANTOWITZ AND LAWRENCE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Barco
FDA UDI
Barco NV·05415334025158·MDRC-2321 SNIB HLX
N/A
FDA UDI
Tyber Medical, LLC·M695M9303150·
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515238022·Cottle Joseph Dbl Hk, two prng, 12mm 5 3/8"
IPULSE HAIR REMOVAL SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFICATION TO ULTROID HEMORRHOID MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INFUSOMAT®
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FPA·June 19, 2024
SUPERDIMENSION INREACH BRONCHUS SYSTEM (SDBS)
FDA Adverse Event
Malfunction
·SUPERDIMENSION INC.·Product code JAK·November 18, 2010
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·January 23, 2013
TECNIS
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HQL·July 11, 2014
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x35 mm Catalog Number: 18965035S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Enforcement
Class II
·Terminated·Stryker GmbH·June 24, 2020