Synthes Falcon Spacers

FDA registration

Synthes (USA) Products LLC·1 product·🇺🇸 United States

FALCON SPACER

FDA 510(k)

FDA Class 2 ·Orthopedic

n.a.

FDA UDI

Karl Storz GmbH & Co. KG·04048551054338·Speculum Holder, for 723018

High Flow Insufflation Unit

FDA registration

SHIRAKAWA OLYMPUS CO., LTD.·3 products·🇯🇵 Japan

WECK VISTA

FDA registration

Teleflex LLC (NADC)·1 product·🇺🇸 United States

Weck

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

High Flow Insufflation Unit

FDA registration

OLYMPUS MEDICAL SYSTEMS CORP.·3 products·🇯🇵 Japan

WECK VISTA

FDA registration

Teleflex Medical LLC·1 product·🇺🇸 United States

WECK VISTA

FDA registration

Teleflex Medical de Tecate, S. de R.L de C.V.·1 product·🇲🇽 Mexico

InfraredX

FDA registration

MICROTEK DOMINICANA, S.A.·3 products·🇩🇴 Dominican Republic

Imaging System

FDA registration

Sterigenics U.S., LLC·3 products·🇺🇸 United States

LenSx Laser System

FDA registration

Sterigenics US LLC·3 products·🇺🇸 United States

WECK VISTA OPTICAL BLADELESS LAPAROSCOPIC ACCESS PORT

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS

FDA 510(k)

FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Catheter, Recording, Electrode, Reprocessed

FDA classification

FDA Class 2 ·Catheter, Recording, Electrode, Reprocessed

Laparoscope, General & Plastic Surgery

FDA classification

FDA Class 2 ·Laparoscope, General & Plastic Surgery