Identity Imprint Porous CR KRS

FDA registration

ConforMIS, Inc.·4 products·🇺🇸 United States

Identity Imprint Porous Total Knee Replacement System, Identity Imprint Porous Cruciate Retaining Total Knee Replacement System

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

Tripod Wrist Lacer

FDA UDI

MEDICAL SPECIALTIES INCORPORATED·00802357233168·

Heine Optotechnik GMBH & Co

FDA registration

TOYO MEDICAL CO.·2 products·🇺🇸 United States

60-ME0236 Pointe Methadone Level 2 Control (375 ng/mL)

FDA registration

HORIBA INSTRUMENTS INCORPORATED·2 products·🇺🇸 United States

Ophthalmoscope, ac-powered

FDA registration

SONTEC INSTRUMENTS, INC.·2 products·🇺🇸 United States

Propoxyphene DAU Calibrators

FDA registration

LIN-ZHI INTERNATIONAL, INC.·2 products·🇺🇸 United States

HEINE OPTOTECHNIK GMBH & CO. KG.

FDA registration

HEINE OPTOTECHNIK GMBH & CO. KG.·2 products·🇩🇪 Germany

(KD2335, KD2328, KD233, KD2337, KD2331, EB-2328A, DL015, DL008)

FDA registration

ZHONGSHAN KINGDOM ELECTRICAL APPLIANCE CO., LTD.·1 product·🇨🇳 China

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167310223316110·

Life Scope® BSM 6000 Series Bedside Monitoring Systems

FDA registration

NIHON KOHDEN TOMIOKA PRODUCTION CENTER·1 product·🇯🇵 Japan

IPL Hair Removal Device (Model: ZHF-IPL-II, ZHF-IPL-III)

FDA registration

Shenzhen Goodwind Technology Development CO., LTD·1 product·🇨🇳 China

Life Scope® BSM 6000 Series Bedside Monitoring Systems

FDA registration

NIHON KOHDEN AMERICA, INC.·1 product·🇺🇸 United States

Life Scope® BSM 6000 Series Bedside Monitoring Systems

FDA registration

Nihon Kohden Corporation - Eastern Japan Logistics Center·1 product·🇯🇵 Japan

Life Scope® BSM 6000 Series Bedside Monitoring Systems

FDA registration

NIHON KOHDEN CORP.·1 product·🇯🇵 Japan

Symphony Thrombectomy System

FDA registration

PDV MedTech·2 products·🇺🇸 United States

HEINE OMEGA 500

FDA 510(k)

FDA Class 2 ·Ophthalmic

SINGLE ANALYTE URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS

FDA 510(k)

FDA Class 2 ·Clinical Toxicology

308-20-INT - DOUBLE DRILL GUIDE diam.2 mm x diam.1.5 mm

FDA registration

GM DOS REIS INDUSTRIA E COMERCIO LTDA·1 product·🇧🇷 Brazil