23 results · 21ms · Sources: EU EUDAMED, US FDA

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EYE TRAY

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

REVELATION DIAMOND

FDA UDI
Ss White Burs, Inc.·D6909121052·REVELATION DIAMOND 811-037SC - 5 PACK

NA

FDA UDI
Stryker Leibinger GmbH & Co. KG·34546540244339·BONE SCREWS, CROSS-FIT, SELF-TAPPING

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756021197·FINGER SPLINTS

Gen. Acces/ Instr. Tip Guard

FDA UDI
KATENA PRODUCTS, INC.·00841668110843·TIP GUARDS VENTED ASSORTED PACK OF 100

Oph. Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668122235·Gills/Welsh Cannula, 25g Angled 9mm Tip

Malibu

FDA UDI
Seaspine Orthopedics Corporation·10889981080525·Bone Probe, Extended Curved

McKesson

FDA UDI
MCKESSON MEDICAL-SURGICAL INC.·20612479275885·MASK, PROC LOOPS ASTM1 BLUE

Arthrex®

FDA UDI
ARTHREX, INC.·00888867057456·UNIVERSAL GLENOID - INLAY MEDIUM PLUS

Innonix Antiviral Child's Face Mask

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

POLYVAC SURGICAL INSTRUMENT DELIVERY SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·July 6, 2017

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·July 6, 2017

SERVO-I

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·May 13, 2014

REPLACEMENT HEART VALVE

FDA Adverse Event
Death ·EDWARDS LIFESCIENCES·Product code DYE·December 1, 2010

NON AC-POWERED PATIENT LIFT

FDA Adverse Event
LAND AMERICA HEALTH & FITNESS·Product code FSA·January 11, 2013

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017

INJECTOR N35-O

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FPA·January 7, 2021

GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·October 20, 2017