20 results
·
19ms
·
Sources: EU EUDAMED, US FDA
ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756016032·ARM SLING
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868032011·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868032035·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868031984·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868032059·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868032042·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868032028·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868031991·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868031977·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868031960·
A.R.T.™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868032004·
ARCHITECT C8000 SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JJE·March 13, 2014
ABSORBABLE SYNTHETIC SUTURE WITH NEEDLE ATTACHMENT (PGA BRAIDED)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VISION R/F TILTING TABLE
FDA 510(k)
FDA Class 2
·Radiology
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962158647·SPOON CURETTE, 5", #2, ANG 25° TIP
UNSPECIFIED BY THE COMPLAINANT
FDA Adverse Event
Injury
·COOK BIOTECH, INCORPORATED·Product code PAG·April 3, 2014
SCREW
FDA Adverse Event
Injury
·Product code HWC·October 17, 2012
FREESTYLE
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code NBW·September 28, 2007
Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021