HemiCAP® MTP Resurfacing Hemi-Arthroplasty Implant

FDA registration

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

HEMICAP MTP RESURFACING HEMI-ARTHROPLASTY IMPLANT

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Toe, Hemi-, Phalangeal

FDA classification

FDA Class 2 ·Prosthesis, Toe, Hemi-, Phalangeal

CA-620

FDA registration

Sysmex America, Inc.·1 product·🇺🇸 United States

ULTRABRAID

FDA registration

SMITH & NEPHEW INC.·1 product·🇺🇸 United States

CA-620

FDA registration

SYSMEX CORPORATION·1 product·🇯🇵 Japan

CA-620

FDA registration

SYSMEX CORPORATION TECHNO PARK·1 product·🇯🇵 Japan

CA-620

FDA registration

Sysmex America, Inc. - Vernon Hills·1 product·🇺🇸 United States

ULTRABRAID

FDA registration

Arthrocare Corporation·1 product·🇨🇷 Costa Rica

CA-620

FDA registration

Sysmex RA Co., LTD, Main Office·1 product·🇯🇵 Japan

ULTRABRAID

FDA registration

SMITH & NEPHEW INC.·1 product·🇺🇸 United States

ULTRABRAID

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

Arthocare8208 (CR2) - ULTRABRAID II 2 BLUE SUTURE 38

FDA registration

Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica

EUROSPITAL S.P.A.

FDA registration

EUROSPITAL S.P.A.·1 product·🇮🇹 Italy

SMITH & NEWPHEW ULTRABRAID II SUTURE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SYSMEX AUTOMATED COAGULATION ANALYZER CA500 SERIES (CA-510, -520, -530, -540. -550, AND -560

FDA 510(k)

FDA Class 2 ·Hematology

Instrument, Coagulation, Automated

FDA classification

FDA Class 2 ·Instrument, Coagulation, Automated

Suture, Nonabsorbable, Synthetic, Polyethylene

FDA classification

FDA Class 2 ·Suture, Nonabsorbable, Synthetic, Polyethylene