Medical device makerLabelled 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 Pivot Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 23, 2015: CinchLock Flex Knotless Suture Anchor.
| Jul 23, 2015 | CinchLock Flex Knotless Suture AnchorK151314 · MBI | 510(k) clearances |
| Oct 7, 2013 | CINCHLOCK KNOTLESS SUTURE ANCHOR, NANOTACK SUTURE ANCHOR 1.4MMK131769 · MBI | 510(k) clearances |
| Mar 14, 2013 | NANOTACK SUTURE ANCHOR 1.4MM WITH FLEX INSERTERK130351 · MBI | 510(k) clearances |
| Feb 21, 2013 | CINCHLOCK KNOTLESS SUTURE ANCHORK123651 · MBI | 510(k) clearances |
| May 25, 2011 | NANOTACK SUTURE ANCHOR 1.4MMK110473 · MBI | 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
