MagniFuse Bone Graft

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States

MagniFuse Bone Graft

FDA registration

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

MagniFuse Bone Graft

FDA registration

OSTEOTECH, INC.·1 product·🇺🇸 United States

GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM SALT BONE VOID FILLER DEVICES

FDA 510(k)

FDA Class 2 ·Orthopedic

Hygrovent Gold

FDA registration

FLEXICARE MEDICAL (DONGGUAN) LTD.·1 product·🇨🇳 China

Prowaterflex

FDA registration

ASAHI INTECC (THAILAND) CO., LTD.·1 product·🇹🇭 Thailand

Prowaterflex

FDA registration

ASAHI INTECC HANOI CO., LTD.·1 product·🇻🇳 Vietnam

Hygrovent Gold

FDA registration

FLEXICARE MEDICAL LTD.·1 product·🇬🇧 United Kingdom

Prowaterflex

FDA registration

ASAHI INTECC CO., LTD.·1 product·🇯🇵 Japan

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450181973·

CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SURGICAL SYSTEM WITH CRYOGUIDE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Filler, Bone Void, Calcium Compound

FDA classification

FDA Class 2 ·Filler, Bone Void, Calcium Compound

Prosthesis, Hip, Cement Restrictor

FDA classification

FDA Class 2 ·Prosthesis, Hip, Cement Restrictor

Unit, Cryosurgical, Accessories

FDA classification

FDA Class 2 ·Unit, Cryosurgical, Accessories