Company · US
Acuitive Technologies, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2024. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 6, 2024 | K240450 | Citrepore Acuitive Technologies, Inc. | MQV |
| Sep 20, 2023 | K232592 | CITRELOCK® DUO Acuitive Technologies, Inc. | MBI |
| Feb 14, 2023 | K221468 | Citregen Tendon Interference Screw (TIS), Citrelock Tendon Fixation Device, Citrespline and Citrelock ACL Implants Acuitive Technologies, Inc. | MAI |
| Nov 4, 2022 | K220833 | Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL Acuitive Technologies, Inc. | MAI |
| Feb 24, 2021 | K210239 | CITRESPLINE and CITRELOCK ACL Implants Acuitive Technologies, Inc. | MAI |
| Feb 5, 2021 | K203334 | The Citrefix Knotless Suture Anchor Acuitive Technologies, Inc. | MAI |
| Oct 7, 2020 | K200725 | Citregen Tendon Interference Screw and Citrelock Acuitive Technologies | MAI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||