35 results · 27ms · Sources: EU EUDAMED, US FDA

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Dornier Medilas H Solvo 35 Laser

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

Maestro™ Total Wrist

FDA UDI
Biomet Orthopedics, LLC·00887868239755·

MAESTRO TOTAL WRIST

FDA UDI
Biomet Orthopedics, LLC·00880304479524·

VARIABLE LOCK SCREW 4.75X35MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWJ·January 24, 2018

Kalitec Universal Instruments

FDA UDI
Kalitec Direct LLC·B07301K1103500·Tray, Base, 3.5", Arcamed

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197453080·CCR Titanium Lateral Blade 24x50m...

All Poly Monotrial

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215063818·

KNEEHAB XP

FDA 510(k)
FDA Class 2 ·Neurology

HOVEROUND TEKNIQUE GT POWER WHEELCHAIR, MODEL# TEKNIQUE GT

FDA 510(k)
FDA Class 2 ·Physical Medicine

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·July 31, 2020

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·December 4, 2019

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·April 30, 2021

SURESTEP

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CGA·October 28, 1998

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·August 31, 2020

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·February 21, 2019

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 16, 2022

T:SLIM G5 SYSTEM

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OYC·October 22, 2019

LOCKING SCREW, FULLY THREADED 5X55 MM

FDA Adverse Event
Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 30, 2010

ACCU-CHEK SPIRIT

FDA Adverse Event
Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·December 11, 2009

OT VERIO PRO METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 18, 2012