Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Valeris Medical with 4 510(k) clearances and 2 device recalls. The most recent is a 510(k) clearance dated Mar 26, 2020: Bonecam Suture Anchor.
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, 2020 | Bonecam Suture AnchorK193108 · MBI | 510(k) clearances |
| Mar 11, 2020 | Apollo Suture Anchor SystemK192810 · MBI | 510(k) clearances |
| Jul 16, 2018 | Valeris Medical Apollo Medial Suture Anchor, Catalog Number MSA-4515, 4.5 x 15mm, each package contains (1) PEEK Screw, (1) #2 ForceBraid BlClass II · The product was mislabeled as containing the incorrect type of suture. | Device recalls |
| Jan 22, 2018 | Apollo XT Suture Anchor, 5.5 x 15 Product Usage: Apollo XT Suture Anchors are intended for: Shoulder - Rotator Cuff Repair - Bankart RepClass II · The label on Apollo XT 5.5mm Suture Anchor (part # XTS-5515; lots 2358, 2362, and 2363) indicated that the anchor screw | Device recalls |
| Nov 16, 2015 | BoneCam Suture AnchorsK152255 · MBI | 510(k) clearances |
| Sep 10, 2014 | Apollo Suture Anchor System and Titan ScrewsK142230 · 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
