Light, surgical, fiberoptic

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA.

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Light, Surgical, Fiberoptic

FDA classification

FDA Class 2 ·Light, Surgical, Fiberoptic

GC Initial™

FDA UDI

Gc America Inc.·15400556708276·GC Initial™ Zr-FS Frame Modifier FM-5, 20g

GC Initial™

FDA UDI

Gc America Inc.·J0228750051·GC Initial™ Zr-FS Frame Modifier FM-5, 20g

D185254

FDA registration

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

CPS02

FDA registration

GVS TM, INC.·1 product·🇺🇸 United States

Ophthalmic Cannula

FDA UDI

KATENA PRODUCTS, INC.·00841668109496·BISHOP-HARMON SILICONE BULB AND ADAPTOR

Arthrex

FDA UDI

Provision·B504OMAR8750050·

Arthrex®

FDA UDI

ARTHREX, INC.·00888867263703·PRFL DRL, 5.0MM CMPR FT

FIBER MESH

FDA 510(k)

FDA Class 2 ·Dental

BROOKER ACETABULAR CUP

FDA 510(k)

FDA Class 2 ·Orthopedic

Arthrex®

FDA UDI

ARTHREX, INC.·00888867319578·PRFL DRL, 5.0MM LG CMPR FT SCRW, REUSE

Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

FDA classification

FDA Class 2 ·Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form