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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

NEPTUNE WASTE MANAGEMENT SYSTEM

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

NA

FDA UDI
Richard Wolf GmbH·04055207045107·OBTURATOR FOR VAGINOSCOPE OD 16.9MM for WL 200...

ReLine

FDA UDI
Nuvasive, Inc.·00195377080523·RELINE C Drill Guide, 14mm Static

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690189671·AK3 AP 4 IN 1 CUTTING GUIDE SIZE 6+

MEDICALGORITHMICS REAL-TIME ECG MONITOR AND ARRHYTHMIA DETECTOR, MODEL POCKETECG

FDA 510(k)
FDA Class 2 ·Cardiovascular

Cronus HP PTA Balloon Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·VASCULAR SOLUTIONS DUETT SEALING DEVICE

NexGen®

FDA UDI
Zimmer, Inc.·00889024224254·

NexGen®

FDA UDI
Zimmer, Inc.·00889024224292·

NexGen®

FDA UDI
Zimmer, Inc.·00889024224278·

NexGen®

FDA UDI
Zimmer, Inc.·00889024224285·

NexGen®

FDA UDI
Zimmer, Inc.·00889024224308·

NexGen®

FDA UDI
Zimmer, Inc.·00889024224339·

NexGen®

FDA UDI
Zimmer, Inc.·00889024224261·

NexGen®

FDA UDI
Zimmer, Inc.·00889024224315·

NexGen®

FDA UDI
Zimmer, Inc.·00889024224322·

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·VASCULAR SOLUTIONS DUETT SEALING DEVICE

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·DUETT PRO SEALING DEVICE AND DIAGNOSTIC DUETT PRO SEALING DEVICE

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·VASCULAR SOLUTIONS DUETT SEALING DEVICE

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·DIAGNOSTIC DUETT