772 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VagiVital Aktivgel
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
TREGOR®
FDA UDI
ASTON MEDICAL·03663703000127·Uncemented standard cup
Treace Medical Concepts
FDA UDI
Provision·B504OM02000980·
DEBAKEY NEEDLE PULLING FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896059665·DEBAKEY NEEDLE PULLING TISSUE FORCEPS TUNGSTEN ...
Lapiplasty SpeedPlate
FDA UDI
Treace Medical Concepts, Inc.·00810111222105·Threaded Rods
GEN4 DIGITAL
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828160346·GEN4 DIGITAL
Initia Total Hip System
FDA UDI
KYOCERA CORPORATION·04547898307195·STDHO LINER 28-48
Initia Total Hip System
FDA UDI
KYOCERA MEDICAL CORPORATION·04580810057679·"STDHO LINER 28-48
Size:28-48
Type:Flat, HO
28m...
Minuteman
FDA UDI
Spinal Simplicity, LLC·M9432000980000·Pathfinder
PLASMALIPO/PLASMA D30 LSER SURGICAL DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SOFTLINE SPRING CLIP
FDA 510(k)
FDA Class 2
·Cardiovascular
COBAS E411 RACK SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·October 15, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011
TI COLLAR WITH GROOVES
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·July 1, 2013
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 21, 2021