KLS Martin SE & Co. KG

FDA registration

KLS Martin SE & Co. KG·1 product·🇩🇪 Germany

KLS-Martin L.P.

FDA registration

KLS-Martin L.P.·1 product·🇺🇸 United States

KLS Martin L1 MMF System

FDA 510(k)

FDA Class 2 ·Dental

SYNTHES XRL; K103320

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

ACS

FDA UDI

AMERICAN CONTRACT SYSTEMS, INC.·00191072015785·RETINAL PACK 173320

ACS

FDA UDI

AMERICAN CONTRACT SYSTEMS, INC.·00191072213631·RETINAL PACK 173320

ACS

FDA UDI

AMERICAN CONTRACT SYSTEMS, INC.·00191072155740·RETINAL PACK 173320

ACS

FDA UDI

AMERICAN CONTRACT SYSTEMS, INC.·00191072189257·RETINAL PACK 173320

ACS

FDA UDI

AMERICAN CONTRACT SYSTEMS, INC.·00191072075956·RETINAL PACK 173320

CENTRONAIL TITANIUM UNIVERSAL FEMORAL NAILING SYSTEM

FDA UDI

ORTHOFIX SRL·18032937168026·CANNULATED SCREW DRIVER

Medisafe® Pill & Med Reminder Application

FDA registration

MEDISAFE PROJECT LTD·1 product·🇮🇱 Israel

SYnthes XRL

FDA registration

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

08.807.223S

FDA registration

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

Jabil Tuttlingen Manufacturing GmbH

FDA registration

Jabil Tuttlingen Manufacturing GmbH·1 product·🇩🇪 Germany

Jabil Switzerland Manufacturing GmbH (Hagendorf)

FDA registration

Jabil Switzerland Manufacturing GmbH (Hagendorf)·1 product·🇨🇭 Switzerland

SYNTHES XRL

FDA registration

SYNTHES GMBH·1 product·🇨🇭 Switzerland

Jabil Inc. (Monument)

FDA registration

Jabil Inc. (Monument)·1 product·🇺🇸 United States

SYNTHES XRL

FDA registration

Synthes GMBH·1 product·🇨🇭 Switzerland

Intervertebral fusion device with bone draft, cervical

FDA registration

SpineSmith Holdings, LLC·1 product·🇺🇸 United States

Spine Smith 0101-0105 Cimplicity: PEEK Lordotic (5°) Implant 13mm(W) x 10mm(D) x 10.5mm(H)

FDA registration

BANISTER TOOL, INC.·1 product·🇺🇸 United States