Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Anika Therapeutics, Inc.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12
Categories6
Latest FDA decision2025-10-15

SEC Filings: 1 filings on record. Latest: 8-K (2026-07-29). View on SEC EDGAR →

TypeNumberDevice NameCodeDateActions
PMA P000046 AID, SURGICAL, VISCOELASTICLZP2025-10-15 View
510(k) K250997 Integrity™ ImplantOWX2025-06-17 View
510(k) K231968 Tactoset® Injectable Bone SubstituteMQV2023-12-20 View
510(k) K223538 Integrity ImplantOWX2023-08-17 View
PMA P090031 Acid, hyaluronic, intraarticularMOZ2023-08-08 View
510(k) K223860 Integrity™ Bone Staple Fixation SystemMBI2023-05-22 View
510(k) K222487 Anika Tissue Tack Fixation SystemGDW2023-05-08 View
510(k) K223915 TactosetMQV2023-03-29 View
PMA P030019 Acid, hyaluronic, intraarticularMOZ2022-11-08 View
510(k) K212083 Tactoset Injectable Bone SubstituteMQV2021-08-31 View
510(k) K190956 SCS 17-01MQV2020-01-30 View
510(k) K173008 SCS 17-01MQV2017-12-26 View

Related Clinical Trials