10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
TRADITION P, PUSH BUTTON HANDPIECE
FDA 510(k)
FDA Class 1
·Dental
Eye Shield
FDA UDI
KATENA PRODUCTS, INC.·00841668111178·EYE SHIELD CLEAR PLASTIC PACK OF 12
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197077460·Ribbon Retractor
50 x 3...
CAP PLUS
FDA 510(k)
FDA Class 2
·Orthopedic
Advance Medical Designs, Inc. Sterile Ultrasound Gel
FDA 510(k)
FDA Class 2
·Radiology
REGEN/RNGLC+ MULTI 66MM SZ 26
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 29, 2017
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2014
RESOLUTE INTEGRITY RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·February 15, 2013
CXD II
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - LARGO·Product code KDJ·January 18, 2011
BIOMET StageOne Knee Tibial Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 433175.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020