70 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Greene Renal Transplant Stent Set
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Comprehensive® Reverse Shoulder
FDA UDI
Biomet Orthopedics, LLC·00880304555389·
ALTRX NEUT 32IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 28, 2019
DELTA CER HEAD 12/14 32MM +1
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LZO·August 28, 2019
BARRX MODELS HALO360 AND HALO360+ COAGULATION CATHETERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SOLITARIE PEEK ANTERIOR SPINAL SYSTEM-TO BE CALLED COLITAIRE 35
FDA 510(k)
FDA Class 2
·Orthopedic
UNKNOWN GLENOSPHERE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·May 22, 2026
COMP RVRS 25MM BSPLT HA+ADPTR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·May 22, 2026
COMP LK SCR 3.5HEX 4.75X20 ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·May 17, 2018
COMP LK SCR 3.5HEX 4.75X20 ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·May 17, 2018
ARCHITECT HAVAB-G
FDA Adverse Event
Malfunction
·ABBOTT GERMANY·Product code LOL·June 20, 2013
MINICAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 27, 2011
1.55MM X 10MM FLUTED TWIST DRL
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 17, 2014
COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·February 18, 2017
COMP LK SCR 3.5HEX 4.75X20 ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·November 26, 2019
COMP RVS CNTRL 6.5X20MM ST/RST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HWC·November 26, 2019
COMP RVRS 25MM BSPLT HA+ADPTR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·November 26, 2019
COMP NLK SCR 3.5HEX 4.75X20 ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·November 26, 2019
COMP LK SCR 3.5HEX 4.75X15 ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·November 26, 2019
ARCOM XL 44-36 STD HMRL BRNG
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·June 30, 2022