9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
PROTEINMETER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Shoreline ACS
FDA UDI
Seaspine Orthopedics Corporation·10889981142841·Trial Rasp 16x14x12mm, 7 Deg Lordosis
REVLITE Q-SWITCHED ND:YAG LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CLINISTAT TDA SERIES
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BZE·December 22, 2009
EVERA XT VR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 10, 2014
SENSIA DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NVZ·October 9, 2010
TOTALCARE BARIATRIC PLUS
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·November 1, 2012
Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024