24 results · 17ms · 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.

SOLO BAND LIGATOR

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Nexxis OR

FDA UDI
Barco NV·05415334002388·NEXXIS SYSTEM X670 CM

NA

FDA UDI
Yeti Dentalprodukte GmbH·EYET3960020·

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600201·Mand. 2. Molar band W-Fit left 20

Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

FDA Pre-Market Approval
FDA Class 3 ·RELIANCE URINARY CONTROL INSERT AND SIZING DEVICE

JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937507·Percutaneous Transluminal Angioplasty Balloon C...

JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939846·Percutaneous Transluminal Angioplasty Balloon C...

JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955938672·Percutaneous Transluminal Angioplasty Balloon C...

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600200501·Mand. 2. Molar band W-Fit left 20

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600200051·Mand. 2. Molar band W-Fit left 20

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600200101·Mand. 2. Molar band W-Fit left 20

Captiva Spine and CapLOX II/TowerLOX Pedicle Screw System

FDA 510(k)
FDA Class 2 ·Orthopedic

AUTOQUANT PLUS

FDA 510(k)
FDA Class 2 ·Radiology

Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

FDA Pre-Market Approval
FDA Class 3 ·RELIANCE URINARY CONTROL INSERT & SIZING DEVICE

NexGen® Legacy®

FDA UDI
Zimmer, Inc.·00889024445437·

NexGen® Legacy®

FDA UDI
Zimmer, Inc.·00889024445468·

NexGen® Legacy®

FDA UDI
Zimmer, Inc.·00889024445444·

NexGen® Legacy®

FDA UDI
Zimmer, Inc.·00889024445451·

NexGen® Legacy®

FDA UDI
Zimmer, Inc.·00889024445475·

INSTRUMENT GENESIS RSP 150/8

FDA Adverse Event
Malfunction ·TECAN SCHWEIZ·Product code JQW·May 29, 2014