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 6 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Surgical Specialties Corporation with 41 510(k) clearances and 1 device recall. The most recent is a device recall dated Mar 26, 2024: POLYSIN (Polyglycolic Acid) suture, HSM9 5-0 BR PGA Part Number G503N.
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.
| Mar 26, 2024 | POLYSIN (Polyglycolic Acid) suture, HSM9 5-0 BR PGA Part Number G503NClass II · Complaints have been received with allegations of Incorrect Needle Curvature. | Device recalls |
| Jul 13, 2016 | LOOK PTFE SutureK160744 · NBY | 510(k) clearances |
| Jul 30, 2014 | QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGNK141778 · GAM | 510(k) clearances |
| Jul 18, 2014 | POLYSYN SURGICAL SUTUREK141625 · GAM | 510(k) clearances |
| Jul 11, 2014 | QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICEK141558 · GAM | 510(k) clearances |
| Feb 28, 2014 | MONODERM SURGICAL SUTUREK140227 · GAM | 510(k) clearances |
| Nov 29, 2013 | TRANQUILL BARBED DEVICEK133420 · NEW | 510(k) clearances |
| Aug 23, 2013 | QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGNK132268 · NEW | 510(k) clearances |
| May 16, 2013 | SHARPOINT POLYPROPYLENE SURGICAL SUTURE, LOOK POLYPROPYLENE SURGICAL SUTURE, QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSUREK131224 · GAW | 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
