19 results
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31ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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VALVED TEARWAY INTRODUCER
FDA 510(k)
FDA Class 2
·Cardiovascular
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036029203·
MILLENNIUM
FDA UDI
Avalign Technologies, Inc.·00190776292690·Molt Periosteal Elevator, #9
CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
APC PLUS ADHESIVE
FDA 510(k)
FDA Class 2
·Dental
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·November 15, 2013
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK USA, INC.·Product code KWP·October 30, 2019
APC PLUS, CLARITY, MINI UNI-TWIN, VICTORY SERIES
FDA Adverse Event
Injury
·3M UNITEK·Product code DYH·May 9, 2012
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 26, 2020
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·April 30, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 14, 2020
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·April 30, 2018
28MM COCR MODULAR HEAD +6MM NO SKIRT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 2, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 15, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 16, 2011
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 8, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·February 2, 2021
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 8, 2017
OPTETRAK ASY,CR CEMENTED FEMORAL, SZ 2,
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 4, 2024