74 results · 42ms · Sources: EU EUDAMED, US FDA

INTERNATIONAL STERILIZATION LABORATORY, LLC

FDA registration
INTERNATIONAL STERILIZATION LABORATORY, LLC·1 product·🇺🇸 United States

NEW DEANTRONICS TAIWAN LTD.

FDA registration
NEW DEANTRONICS TAIWAN LTD.·1 product·🇹🇼 Taiwan

Valleylab™ Laparoscopic Wire J-Hook Electrode Retractable, Aspiration Holes, 28 cm, E3782R-28ASP

FDA registration
Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

Valleylab™ Laparoscopic Wire J-Hook Electrode, Hollow,28cm, E3782-28

FDA registration
Covidien·1 product·🇺🇸 United States

Laparoscopic Curved Spatula Electrode, Retractable, Aspiration Hole, 28cm ; Laparoscopic Wire J-Hook Electrode, Retractable, Aspiration Hole, 28cm ; Laparoscopic Wire L-Hook Electrode, Retractable, Aspiration Hole, 28cm; Laparoscopic Wire L-Hook Electrode, Retractable, Aspiration, 36cm ; Laparoscopic Flat L-Hook Electrode, Retractable, Aspiration Hole, 28cm ; Laparoscopic Straight Spatula Electrode, Hollow, 28cm ; Laparoscopic Curved Spatula Electrode, Hollow, 28cm; Laparoscopic Wire J

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

Collis-Curve Toothbrush

FDA registration
Collis Curve Toothbrush·1 product·🇺🇸 United States

Vanguard® Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304271760·

Hollister (WP) -VaPro Pocket (20cm)

FDA registration
Synergy Health Westport Ltd·1 product·🇮🇪 Ireland

VaPro Pocket (20cm/8 inch)

FDA registration
HOLLISTER ULC·1 product·🇮🇪 Ireland

VaPro Pocket (20cm/8 inch)

FDA registration
Hollister Services BV·1 product·🇳🇱 Netherlands

Ponto bone anchored hearing system

FDA registration
Oticon Medical AB·1 product·🇸🇪 Sweden

VaPro Pocket (20cm/8 inch)

FDA registration
HOLLISTER INCORPORATED·1 product·🇺🇸 United States

Ponto bone anchored hearing system

FDA registration
Demant Operations Poland Sp. z o.o.·1 product·🇵🇱 Poland

EZ HSG CATHETER.FOAMSEAL CATHETER

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

PONTO PRO POWER

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

ART - Arthrex Eclipse™ Trial Head (AR-94XX-XX), Device Listing: D354030

FDA registration
PERRYMAN COMPANY·1 product·🇺🇸 United States

ARTHREX, INC.

FDA registration
ARTHREX, INC.·2 products·🇺🇸 United States

Straumann cerabone

FDA registration
BOTISS BIOMATERIALS GMBH·1 product·🇩🇪 Germany

MARLE FINISHING SAS

FDA registration
MARLE FINISHING SAS·2 products·🇫🇷 France

Eclipse Implants

FDA registration
GB IMPLANTAT TECHNOLOGIE GMBH·2 products·🇩🇪 Germany