# Acuitive Technologies, Inc.

- Location (FDA's records): Alendale, NJ
- FDA decisions: 7 (2020–2024): 7 510(k) clearances
- Names in FDA's records: Acuitive Technologies, Inc. (6); Acuitive Technologies (1)
- Product codes: MAI (5), MQV (1), MBI (1)
- 510(k) review time since 2016: median 202 days, against 78 for FDA's reviews in the same codes and years (3 of 7 faster)
- Predicates its devices cite: 12 (9 its own); citations of its devices by later devices: 9 (9 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrex, Inc.: 2 (https://510kreport.com/company/arthrex)
- Orthovita, Inc.: 1 (https://510kreport.com/company/orthovita)

## Its most-cited devices
- K200725: Citregen Tendon Interference Screw and Citrelock (2020), cited by 4
- K210239: CITRESPLINE and CITRELOCK ACL Implants (2021), cited by 2
- K203334: The Citrefix Knotless Suture Anchor (2021), cited by 2
- K220833: Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL (2022), cited by 1

## Recent decisions
- K240450: Citrepore™ (Nov 6, 2024)
- K232592: Citrelock® Duo (Sep 20, 2023)
- K221468: Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device, Citrespline™ and Citrelock™ ACL Implants (Feb 14, 2023)
- K220833: Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL (Nov 4, 2022)
- K210239: CITRESPLINE and CITRELOCK ACL Implants (Feb 24, 2021)
- K203334: The Citrefix Knotless Suture Anchor (Feb 5, 2021)
- K200725: Citregen Tendon Interference Screw and Citrelock (Oct 7, 2020)

Source page: https://510kreport.com/company/acuitive-technologies