Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Incisive Surgical with 5 510(k) clearances and 2 device recalls. The most recent is a device recall dated Aug 29, 2018: INSORB SUBCUTICULAR SKIN STAPLER, REF 2030.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 29, 2018 | INSORB SUBCUTICULAR SKIN STAPLER, REF 2030Class II · Possible compromise of the sterile barrier integrity | Device recalls |
| Mar 19, 2015 | Insorb Subcuticular Skin Stapler. INSORB staples are made from an absorbable copolymer which is a synthetic polyester derived from lactic aClass II · A previous Turkish distributor over-labeled a portion of the lot with an expiration date of 2016-05. The expiration dat | Device recalls |
| Mar 16, 2012 | INSORB ABSORBALBE STAPLEK120373 · GDW | 510(k) clearances |
| Feb 6, 2009 | INSORB ABSORBABLE STAPLE, MODEL 1020, 1025, AND OTHER PRODUCT FAMILIESK090159 · GDW | 510(k) clearances |
| Jul 26, 2006 | INSORB ABSORBABLE STAPLE, MODEL 1020K061784 · GDW | 510(k) clearances |
| Dec 16, 2003 | INSORB ABSORBABLE STAPLE, MODEL SP-B20K033602 · GDW | 510(k) clearances |
| Apr 22, 2003 | INSORB ABSORBABLE STAPLES, MODEL SP-B20K024117 · GDW | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
