21 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Midwest Rhino XE and Air Motor M
FDA 510(k)
FDA Class 1
·Dental
MIDWEST LOW SPEED ATTACHMENTS - CONTRA ANGLE SHEATH
FDA Adverse Event
Malfunction
·SIRONA DENTAL SYSTEMS GMBH·Product code EFB·April 20, 2023
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260704·
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463073·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694019095·2.4mm x 9mm Cannulated Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070560·Cannulated 2.4 x 9mm Lag Screw Sterile Qty 5
DEFENDO DISPOSABLE AIR/WATER VALVE MODEL 100304
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HYDRO-GUARD MINI BREATHING FILTER AND HEAT AND MOISTURE EXCHANGER AND AIR-GUARD CLEAR BREATHING FILTER
FDA 510(k)
FDA Class 2
·Anesthesiology
ECHO POR FMRL RED NC 9X125MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·May 14, 2019
M/H 3HOLE RLC SHL NRS 56MM/L24
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·May 14, 2019
E-POLY 40MM +3 HIWALL LNR SZ24
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·August 9, 2018
28MM MODULAR HEAD STANDARD NECK TYPE 1 TAPER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·October 4, 2016
INRATIO
FDA Adverse Event
Injury
·HEMOSENSE, INC.·Product code JPA·October 6, 2008
ULTRASONIC DISSECTOR QTY OF 6
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code LFL·June 18, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 5, 2011
M2A-MAGNUM PF CUP 48ODX42ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·December 30, 2022
M2A MAGNUM 42-50M TPR INSRT +9
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 17, 2017
M2A-MAGNUM MOD HD SZ 46MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 17, 2017
STR MOD ACET INSERTER HANDLE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MDM·June 9, 2017
S313142 ZB120201 STRAIGHT MAGNUM INSERTER ¼-20 THREADED ROD KIT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LXH·June 9, 2017