53 results · 27ms · Sources: EU EUDAMED, US FDA

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BIOSPINE VBR SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

JOBST SensiFoot

FDA UDI
BSN MEDICAL, INC.·00035664108649·SENSFOOT 8-15 KH XL NA 1 EN FR ES

Leva® Anterior Interbody System

FDA UDI
Spine Wave, Inc.·10840642108194·Plate, 26 mm/30 mm (W) x 11 mm (H)

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306819131·Retractor, Jordan-Simpson, Right Angled, 1"

KYPHON XPANDER II INFLATABLE BONE TAMP

FDA 510(k)
FDA Class 2 ·Orthopedic

ANALYST PANELS + ANALYTICAL TEST ROTOR

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

CONTOUR

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·December 14, 2012

CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code GEI·November 1, 2015

KYPHOPAK TRAY

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·May 24, 2021

KYPHON XPANDER II INFLATABLE BONE TAMP

FDA Adverse Event
Malfunction ·MEDTRONIC MEXICO·Product code HRX·November 6, 2019

KYPHON XPANDER II INFLATABLE BONE TAMP

FDA Adverse Event
Malfunction ·MEDTRONIC MEXICO·Product code HRX·April 5, 2021

KYPHON XPANDER II INFLATABLE BONE TAMP

FDA Adverse Event
Malfunction ·MEDTRONIC MEXICO·Product code HRX·July 11, 2019

KYPHON XPANDER II INFLATABLE BONE TAMP

FDA Adverse Event
Malfunction ·MEDTRONIC MEXICO·Product code HRX·August 31, 2019

KYPHON XPANDER II INFLATABLE BONE TAMP

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018

PINNACLE PELVIC FLOOR REPAIR KITS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 14, 2013

MINICAP

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 2, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 14, 2008