21 results · 24ms · Sources: EU EUDAMED, US FDA

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FuckWater

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

NA

FDA UDI
KEY SURGICAL, INC.·10849771050077·Steinmann Pins, Double diamond, threaded, 5/64-...

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704294002·

Key Surgical K-Wires and Steinmann Pins

FDA UDI
KEY SURGICAL, INC.·00849771015338·Steinmann Pins, Double diamond, threaded, 5/64-...

SOLID CANCELLOUS LAG SCREW

FDA UDI
Biomet Orthopedics, LLC·00887868005091·

Ophthalmic Ring

FDA UDI
KATENA PRODUCTS, INC.·00841668100783·FLIERINGA FIXATION RING 17MM

OsteoMed

FDA UDI
OSTEOMED LLC·00845694045834·PrimaLIF LLIF PEEK Implant, 17mm X 26mm X 30mm,...

LONGEVITY IT HIGHLY CROSSLINKED POLYETHYLENE CONSTRAINED LINERS

FDA 510(k)
FDA Class 2 ·Orthopedic

STUDIODOP VICORDER

FDA 510(k)
FDA Class 2 ·Cardiovascular

SUMMIT POR TAPER SZ5 HI OFF

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·September 12, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·June 16, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·October 14, 2014

ARTICULEZE M HEAD 36MM +1.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·May 10, 2013

PINNACLE MTL INS NEUT36IDX56OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 10, 2013

PINNACLE SECTOR II CUP 56MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·May 10, 2013

BD SAFETYGLIDE INSULIN SYRINGE

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code MEG·January 25, 2019

HIGHLY CROSSLINKED POLYETHYLENE CONSTRAINED LINER

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code KWZ·September 26, 2016

PINNACLE MTL INS NEUT36IDX54OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code KWA·September 30, 2013

ARTICULEZE M HEAD 36MM +1.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·September 30, 2013