18 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Iridex TruFocus LIO Premiere
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HUMERAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868004827·
Symmetry Mixter
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482035467·Symmetry® Forceps, Mixter Artery, Delicate, 7 1...
MODIFICATION TO: BODYGUARD INFUSION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
AUDIT MICROCV AMMONIAN/ETHANOL LINEARITY SET, MODEL K712M-5
FDA 510(k)
FDA Class 1
·Clinical Chemistry
HNM Medical
FDA UDI
HNM STAINLESS, LLC.·00842962111949·MIXTER ARTERY FORCEPS, 7 1/8", DELICATE
VIDAS® TOXO IGM
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LGD·February 2, 2017
VIDAS® TOXO IGM
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LGD·October 12, 2016
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 14, 2013
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·May 2, 2011
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008
VASERLIPO SYSTEM
FDA Adverse Event
Injury
·SOLTA MEDICAL, INC·Product code QPB·January 9, 2023
BIOZORB
FDA Adverse Event
Injury
·HOLOGIC, INC·Product code NEU·September 6, 2023
VIDAS® TOXO IGM
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LGD·June 9, 2017
VIDAS® TOXO IGM
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LGD·June 9, 2017
VIDAS® TOXO IGM
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LGD·June 15, 2017
VIDAS® TOXO IGM
FDA Adverse Event
Malfunction
·BIOMERIEUX, S.A.·Product code LGD·June 13, 2017
AquaC UNO H [120V, 60Hz, 1000VA, Fresenius US-Version: 24-10VA-1 Vivonic Part Number: G02000970-US
FDA Enforcement
Class II
·Ongoing·Fresenius Medical Care Holdings, Inc.·August 3, 2022