37 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Easy-Load Lens Delivery System
FDA 510(k)
FDA Class 1
·Ophthalmic
Cohere
FDA UDI
Nuvasive, Inc.·00887517014047·COHERE TLIF-O Trial, 16x10mm 12°
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·05019279057580·
ORTHOPEDIC SALVAGE SYSTEM (OSS)
FDA UDI
Biomet Orthopedics, LLC·00880304250772·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311610120·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321610120·
10PC - UP - 380-54620 - Locamotive
FDA UDI
Certified Safety Manufacturing, Inc.·00766588110127·10PC - UP - 380-54620 - Locamotive
V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201
FDA 510(k)
FDA Class 2
·Cardiovascular
AXSOS PLUS LOCKING PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071150358·16F x 1.0cm MiniSPC Low Profile Suprapubic Cath...
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071147730·16F x 1.0cm MiniSPC Low Profile Suprapubic Cath...
ACCELERATOR A3600
FDA Adverse Event
Malfunction
·INPECO SA·Product code JQP·December 20, 2024
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·October 10, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
COULTER LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·June 17, 2011
OSS INTERLOK IM STEM W/SCREW
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·March 23, 2018
CPS SM SPDL WITH PINS 600LBF
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDC·July 31, 2019
OSS RS AXLE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 31, 2019
OSS TIBIAL POLY BEARING 12MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 31, 2019
OSS MOD TIB BASEPLATE 79MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 31, 2019