Profile: Innobiosurg Co.,Ltd is a provider of anker groove products. We are an ISO 13485 certified company. Our anker-groove part anker-groove collects the bone core happened during the fixture implantation and prevents peri-implantitics such as disease issues.
FDA Registration Number: 3008309654
US Agent: April Lee / Withus Group Inc
Phone: +1-(909)-274-9971 E-Mail:
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• Skin Graft Surgical Expander (FDA Code: FZW / 878.4800) A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892. |