89 results · 25ms · Sources: EU EUDAMED, US FDA

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Customized Contour Implant

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Ceramco® iC

FDA UDI
Dentsply International Inc.·D00142006100·C1

ReLine

FDA UDI
Nuvasive, Inc.·00195377047656·RELINE-O Trial, 6mm H Ang Right L-pop

Zodiac

FDA UDI
ALPHATEC SPINE, INC.·00844856023413·SS OFFSET CONNECTOR, 10MM

Zavation

FDA UDI
Zavation LLC·00842166131743·Ti3Z CIF 12mmx14mmx10mm -6 deg

Zodiac

FDA UDI
ALPHATEC SPINE, INC.·00844856002029·OFF CONNECTOR ASSEMBLY 10mm

OsteoMed

FDA UDI
OSTEOMED LLC·00845694007276·M4 Micro Plate Organizer, Aluminum, Series II

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756004329·POST-OP SHOE

Calibration Hose Set for PTS BFR, plastic Female

FDA UDI
Delfi Medical Innovations Inc·M995922006103·Calibration Hose set for the use with PTS BFR T...

LYPHOCHEK WHOLE BLOOD METALS CONTROL MODEL # 527, 528, 529

FDA 510(k)
FDA Class 1 ·Clinical Toxicology

RESOLUTION CHOLESTEROL MONITOR

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

FMS DUO+

FDA Adverse Event
Injury ·FMS GROUP·Product code FRN·December 18, 2006

BREAST IMPLANT

FDA Adverse Event
Malfunction ·MENTOR·Product code FWM·April 6, 2006

APEX MODULAR HIP STEM

FDA Adverse Event
Injury ·OMNI LIFE SCIENCE INX·Product code KWY·June 25, 2008

ACCU-CHEK COMPACT STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 29, 2006

APEX MODULAR HIP STEM

FDA Adverse Event
Injury ·OMNI LIFE SCIENCE, INC.·Product code KWY·August 9, 2006

APEX MODULAR HIP STEM

FDA Adverse Event
Injury ·OMNI LIFE SCIENCE, INC·Product code LPH·August 28, 2008

TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·May 4, 2006

TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·May 4, 2006

TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·May 4, 2006