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 Anika Therapeutics with 11 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Sep 17, 2026: Integrity Retractable Implant Inserter (6000127).
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.
| Sep 17, 2026 | Integrity Retractable Implant Inserter (6000127)K261869 · MBI | 510(k) clearances |
| Sep 2, 2026 | HYALOMATRIXK261311 · QSZ | 510(k) clearances |
| Jun 17, 2025 | Integrity™ ImplantK250997 · OWX | 510(k) clearances |
| Dec 20, 2023 | Tactoset® Injectable Bone SubstituteK231968 · MQV | 510(k) clearances |
| Aug 17, 2023 | Integrity ImplantK223538 · OWX | 510(k) clearances |
| May 22, 2023 | Integrity™ Bone Staple Fixation SystemK223860 · MBI | 510(k) clearances |
| May 8, 2023 | Anika Tissue Tack Fixation SystemK222487 · GDW | 510(k) clearances |
| Mar 29, 2023 | TactosetK223915 · MQV | 510(k) clearances |
| May 10, 2018 | Hyalomatrix, Product nos. 651105, 651103, 651104, and 651301 Product Usage: Hyalomatrix is a bi-layered, sterile, flexible, and comfortaClass II · Hyalomatrix products are susceptible to degradation as a result of the decomposition of PVC in the packaging material du | Device recalls |
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
