14 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Diode Laser Hair Removal (LHR-V6S-1064, LHR-V6S/B-1064)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STRYKER TOTAL PERFORMANCE (TPS) SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Swang-Ganz IQ pulmonary artery catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101542·R E-MAXTM Vitamin E Ultracongruent Tibial Inser...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523145218·R CR UHMWPE Ultracongruent Tibial Insert Sz A 17mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124558·R Ultracongruent Tibial Insert Trial Sz A 17mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102310·R CR MAXTM HXL Ultracongruent Tibial Insert Sz ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523164578·R Ultracongruent Tibial Insert Trial with Anter...
BD NEXIVA¿ DIFFUSICS¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·February 11, 2020
LIFEPAK 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code LDD·November 4, 2008
UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·September 1, 2011
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 17, 2013
23-2117-0 ANIOSGEL 85 NPC HAND SANITIZER 500ML
FDA Adverse Event
Injury
·ANGELINI PHARMA INC.·Product code LRJ·December 22, 2025
23-2117-0 ANIOSGEL 85 NPC HAND SANITIZ 500ML
FDA Adverse Event
Malfunction
·ANGELINI PHARMA INC.·Product code LRJ·January 20, 2026