35 results · 20ms · Sources: EU EUDAMED, US FDA

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OLYMPIC WARM-UP

FDA 510(k)
FDA Class 2 ·Physical Medicine

ODYSSEY®

FDA UDI
Microport Orthopedics Inc.·M684KS0010561·

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00160561·

PowerPICC

FDA UDI
Bard Access Systems, Inc.·00801741225154·Catheter Placement Kit

artVeneer life

FDA UDI
Merz Dental GmbH·D7092001056·artVeneer life lower anteriors, UBXL, A2

AiroDyne M-set 36'' × 80'' QLT Burgundy Tridien

FDA UDI
Tridien Medical·00841965103951·AiroDyne M-set 36'' × 80'' QLT Burgundy Tridien

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·November 12, 2024

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·January 19, 2025

BIO-LIPID HUMAN SERUM HDL AND LDL CALIBRATORS

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

SMART SHIELD NON-STERILE POWDER-FREE PEPPERMINT SCENTED GREEN LATEX EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·October 28, 2024

9616240-2006-00341

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

9616240-2006-00332

FDA Adverse Event
Other ·Product code FII·June 1, 2006

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

9616240-2006-00339

FDA Adverse Event
Malfunction ·Product code FII·June 9, 2006

9616240-2006-00340

FDA Adverse Event
Malfunction ·Product code FII·June 9, 2006

9616240-2006-00350

FDA Adverse Event
Malfunction ·Product code FII·June 23, 2006

9616240-2006-00345

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

CARDIOSAVE HYBRID, TYPE I PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·February 3, 2026

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006