40 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEMOSTATIX THERMAL SCALPEL SYSTEM - #12 BLADE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00120211·
artVeneer life
FDA UDI
Merz Dental GmbH·D7092002021·artVeneer life lower posteriors, XL, A3
LF
FDA UDI
Shenzhen Boon Medical Supply Co., Ltd.·06938327906238·60"(1500 mm) Y Tubing with Dual Check Valves(DE...
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·04546540497895·PERCUTANEOUS SPINE CLAMP (LONG)
L-15 MEDIUM, CATALOG NO. 200-2021
FDA 510(k)
FDA Class 1
·Hematology
EQUINOXE PRIMARY SHOULDER COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·August 25, 2022
SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE C-ARM
FDA 510(k)
FDA Class 2
·Radiology
AESCULAP BONE WAX
FDA 510(k)
FDA Unclassified
·Unknown
BD BBL MGIT MYCOBACTERIA GROWTH INDICATOR TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·January 19, 2021
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·March 27, 2020
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·June 27, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·February 6, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·February 6, 2019
DEXTRUS 4136
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVN·March 13, 2013
PUMP/GRAVITY SOLUTION NO 'Y' SITE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MALTA·Product code FPA·February 27, 2011
ICY HOT HEAT THERAPY PATCH - BACK
FDA Adverse Event
Injury
·CHATTEM, INC.·Product code IMD·February 21, 2008
EQUINOXE REVERSE 38MM HUMERAL LINER +0
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·August 17, 2022
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·June 3, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·July 9, 2019