339 results · 29ms · Sources: EU EUDAMED, US FDA

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Sharps Needle Destruction Device

FDA Pre-Market Approval
FDA Class 2 ·THE DISINTEGRATOR INSULIN NEEDLE DESTRUCTION DEVICE

Sharps Needle Destruction Device

FDA Pre-Market Approval
FDA Class 2 ·THE DISINTEGRATOR PLUS LANCE/INSULIN NEEDLE DESTRUCTON DEVICE

Sharps Needle Destruction Device

FDA Pre-Market Approval
FDA Class 2 ·DISINTEGRATOR PRO NEEDLE DESTRUCTION DEVICE

Armstrong

FDA UDI
MEDTRONIC XOMED, INC.·00763000870508·VENT TUBE 1010040 5PK ARMSTRONG 7MM SIL

Armstrong

FDA UDI
MEDTRONIC XOMED, INC.·00763000038496·VENT TUBE 1010040 5PK ARMSTRONG 7MM SIL

NVJJB

FDA UDI
Nuvasive, Inc.·00887517161307·NVJJB Electrodes, Dual Wet Gel

Armstrong

FDA UDI
MEDTRONIC XOMED, INC.·00681490028134·VENT TUBE 1010040 5PK ARMSTRONG 7MM SIL

PUMA-G System™

FDA UDI
Coaptech, Inc.·00860312001504·Percutaneous Ultrasound Gastrostomy (PUG) Syste...

ENT-single-use suction tubes, angled

FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250676706157·rounded tip, suction control on side 100x4....

Santis Pre Bent Rod 5.5mmx40mm

FDA UDI
Lanterna Medical Technologies GmbH·07640159550556·Santis Pre Bent Rod 5.5mmx40mm

SMALL HUDSON RATCHETING T-HANDLE

FDA UDI
Osteocentric Technologies, Inc.·00810097803848·SMALL HUDSON RATCHETING T-HANDLE

MEGA PLUS SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809763502279·Dual Locking Wrench(Short)

SANTIS™ PRE BENT ROD 5.5mm X40mm -STERILE

FDA UDI
Lanterna Medical Technologies GmbH·07640159551676·SANTIS™ PRE BENT ROD 5.5mm X40mm -STERILE

mahe medical GmbH

FDA UDI
mahe medical gmbh·04050659173279·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...

6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 40/16 mm

FDA UDI
mahe medical gmbh·EMAH00100100400·6.5 Cancellous Bone Shaft Screw, hex, St.Ste...

Integrity-SI Fusion System

FDA UDI
Lincotek Medical LLC·B57112521010040D0·10 x 40 mm Anodized SI Implant

GMA 2.0 Pedicle Screw System

FDA UDI
GRAFTON MEDICAL ALLIANCE, INC.·00810021380223·PRE-BENT ROD, ø5.5 X 40

SLEEVED FILTER

FDA 510(k)
FDA Class 2 ·Anesthesiology

Implanted Fecal Incontinence Device

FDA Pre-Market Approval
FDA Class 3 ·AMS ACTICON NEOSPHINCTER

Device, Thermal Ablation, Endometrial

FDA Pre-Market Approval
FDA Class 3 ·HYDRO THERMABLATOR ENDOMETRIAL ABLATION SYSTEM