Incisive Surgical, Inc.
Incisive Surgical, Inc. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2012, with 2 FDA device recalls on record.
Top product codes for Incisive Surgical, Inc.
FDA recalls by Incisive Surgical, Inc.
- Z-0078-2019 — INSORB SUBCUTICULAR SKIN STAPLER, REF 2030
- Z-1545-2015 — Insorb Subcuticular Skin Stapler. INSORB staples are made from an absorbable copolymer which is a synthetic polyester derived from lactic and glycolic acids. It is chemically similar to other surgical glycolide/lactide-based copolymers. Polyglycolic/polylactic acid copolymers degrade in vivo by hydrolysis to glycolic acid and lactic acid which are then absorbed and metabolized by the body.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Incisive Surgical, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.