20 results · 22ms · Sources: EU EUDAMED, US FDA

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STRYKER LAPAROSCOPE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

R82

FDA UDI
R82 A/S·05707292787286·

R82

FDA UDI
R82 A/S·05707292450807·

MUSE CARDIOLOGY INFORMATION SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4

FDA 510(k)
FDA Class 2 ·Dental

PERFORMANCE MODULAR TIBIAL TRAY SML

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

E1 HI-WALL LINER RINGLOC-X 60MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·January 10, 2017

PERFORMANCE FEMORAL STEM 16X100MM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

POLISHED IBEAM TIB TRAY 71MM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·July 11, 2016

NON-POROUS PERF TIB TRAY-XSML

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·March 23, 2018

POLISHED FINNED TIBIAL TRAY 71 MM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·March 10, 2017

POLISHED FINNED 1 PIECE TIBIAL TRAY

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 12, 2017

POLISHED FINNED TIBIAL TRAY 75MM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·July 10, 2017

EASYTRAK 2

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code OJX·January 11, 2013

COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 30, 2010

SOLETRA

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 2, 2014

MAXIM PRIMARY FEMORAL COMPONENT 75 MM LEFT / POROUS 75 LT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 30, 2017

DCM MAXIM PRIMARY TIBIAL BEARING 12 MM THICK X 71/75 WIDE ARCOM UHMWPE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 30, 2017

ANATOMIC SHOULDER PROSTHESIS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWS·April 23, 2026

ANATOMIC SHOULDER PROSTHESIS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWS·February 16, 2026