25 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ASPIRA PLEURAL DRAINAGE SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Medtronic Reusable Instruments
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902096297·SLEEVE 9110409 SWITCHING 18MM TPRD
Leva® Anterior Expandable Spacer System
FDA UDI
Spine Wave, Inc.·10840642109146·Spacer, 30 mm (W) x 28 mm (D) x 19 mm (H), 15° ...
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100090·Tray Insert 2, Cosmolock, Arcamed
Navagio
FDA UDI
Kalitec Direct LLC·B07330K1100090·Tray Insert
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K1100090·Tray Insert, Level II
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K1100090·Tray Insert
LYNX
FDA UDI
HNM TOTAL RECON LLC·00841742112725·LYNX Distal Fibula Locking Plate, Ti - (L)151mm...
CBC-SF
FDA 510(k)
FDA Class 2
·Hematology
POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTUE ANTERIOR FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
GORE VIABAHN ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·January 14, 2011
GORE VIABAHN ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·January 14, 2011
GORE VIABAHN ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·January 14, 2011
GORE VIABAHN ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·January 14, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 13, 2013
TILDA R 45 US
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVN·September 23, 2014
SECURE 3 MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·April 25, 2011
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 26, 2024
NA
FDA Adverse Event
Malfunction
·STRYKER SUSTAINABILITY SOLUTIONS LAKELAND·Product code NLQ·January 10, 2017
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 15, 2020