9 results
·
23ms
·
Sources: EU EUDAMED, US FDA
LUMIX 70B
FDA 510(k)
FDA Class 2
·Dental
Ophthalmic Forceps
FDA UDI
KATENA PRODUCTS, INC.·00841668106167·HOSKIN #34 COLIBRI FORCEPS SHARP
GE HEALTHCARE INSTA TRAK 3500PLUS/ FLUORO TRAK 9800 PLUS SYSTEM WITH AXCESS BONE PIN, MODEL PART # 1006955
FDA 510(k)
FDA Class 2
·Neurology
ProVee Video Processing Unit (PV-003)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TI COLLAR WITH GROOVES
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code MNI·June 5, 2012
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MPRI·Product code LWS·February 9, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 23, 2014
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·January 6, 2011
Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position.
FDA Recall
Terminated
·Silhouette Lift, Inc.·Product code GAM·July 2, 2015