Cook Incorporated

FDA registration

Cook Incorporated·1 product·🇺🇸 United States

Cook Incorporated

FDA registration

Cook Incorporated·1 product·🇺🇸 United States

AQ HYDROPHILIC UROLOGICAL CATHETERS

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Catheter, Ureteral, Gastro-Urology

FDA classification

FDA Class 2 ·Catheter, Ureteral, Gastro-Urology

YS, YES STUDIO, DonnaMax, Bioswiss. Model: K1, K2, K3, K4, K5, K6, K7, K8, K9, 6200, 6201, 6202, 6203, 6204, 6205, 6206, 6207

FDA registration

CORAL HEALTHCARE PRODUCTS MANUFACTURER CO., LTD.·1 product·🇨🇳 China

HEALING PEEK CAP. NARROW PROF.

FDA registration

SWEDEN & MARTINA S.P.A.·2 products·🇮🇹 Italy

Zeiss 30 SL-L

FDA registration

CARL ZEISS MEDITEC AG (JENA)·1 product·🇩🇪 Germany

APEX Knee System

FDA UDI

Omni Life Science, Inc.·00841690190622·Sizing Guide 3 deg Rotation Bushing -1mm

CHARNLEY

FDA UDI

DEPUY INTERNATIONAL LTD·10603295240532·CHARNLEY PN RETRACT & HANDLE

Menicon Z DW

FDA registration

Menicon Nect Co., Ltd., Gujo Plant·1 product·🇯🇵 Japan

PROTRUSIO CAGE CEMENTED ACETABULAR RECONSTRUCTION 48ODX45ID RT

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

Menicon Z DW

FDA registration

MENICON CO. LTD.·1 product·🇯🇵 Japan

Menicon Z DW

FDA registration

Menicon Co., Ltd., R&D Center·1 product·🇯🇵 Japan

MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT

FDA 510(k)

FDA Class 2 ·Orthopedic

PREMIUM Implant Systems SHELTA Implant Systems

FDA 510(k)

FDA Class 2 ·Dental

Lens, Contact (Rigid Gas Permeable), Extended Wear

FDA Pre-Market Approval

FDA Class 3 ·MENICON Z(TM) (TISILFOCON A) RIGID GAS PERMEABLE CONTACT LENS FOR 30-DAY EXTENDED WEAR

Spinal Vertebral Body Replacement Device

FDA classification

FDA Class 2 ·Spinal Vertebral Body Replacement Device

Abutment, Implant, Dental, Endosseous

FDA classification

FDA Class 2 ·Abutment, Implant, Dental, Endosseous