39 results · 28ms · Sources: EU EUDAMED, US FDA

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SenSmart Model 8203CA Regional Oximetry Sensor (Adult/Pediatric, >40 kg, SenSmart Model 820CA Regional Oximetry Sensor (Adult/Pediatric, >40 kg)

FDA 510(k)
FDA Class 2 ·Cardiovascular

CoRoent

FDA UDI
Nuvasive, Inc.·00887517637918·CoRoent Ant TLIF PEEK, 15x11x30mm 15°

POUR-PLUS

FDA UDI
Denplus Inc·D8451151305·POUR-PLUS, LPI, 11.3 kg

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04064984699571·GENUMEDI PSS BLUE, SIZE V

OMNI Mod Hip

FDA UDI
Omni Life Science, Inc.·00841690102724·OMNI Modular Stem Size 5, 13mm

KIT, TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Injury ·ALERE SAN DIEGO, INC.·Product code MMI·July 19, 2012

HNM SPORTS MEDICINE

FDA UDI
HNM STAINLESS, LLC.·00842962101629·ETHOS PRO SMALL JOINT ANCHOR XL, PEEK, 2.9mm x ...

ARK LAMOTRIGINE ASSAY, CALIBRATOR & CONTROL

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

CS MEDICAL TD-100 TRANSESOPHAGEAL PROBE DISINFECTOR, MODEL TD-100, CS MEDICAL TD-5 HIGH-LEVEL DISINFECTANT, MODEL TD-5

FDA 510(k)
FDA Class 2 ·Radiology

HNM SPORTS MEDICINE

FDA UDI
HNM STAINLESS, LLC.·00842962103777·ETHOS PRO SMALL JOINT ANCHOR XL, PEEK, 2.9mm x ...

EXPECT PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·May 19, 2026

EXPECT PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·September 24, 2025

ACQUIRE? PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·October 10, 2025

EXPECT PULMONARY

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·November 14, 2024

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026

EXPECT PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·April 14, 2026

2.7MM METAPHYSEAL SCR SLF-TPNGW/T8 STRDRV RECESS/26MM

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·June 7, 2013

UNKNOWN DEPUY SZ 5 PS FEMORAL COMPONENT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 30, 2011

SURGISIS BIODESIGN COMPLEX HERNIA GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH INC.·Product code GXQ·September 4, 2008

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·October 7, 2025