# Arc Surgical, LLC

- Location (FDA's records): Hillsboro, OR
- FDA decisions: 5 (2005–2015): 5 510(k) clearances
- Product codes: HWC (3), HTY (1), HAW (1)
- Predicates its devices cite: 15 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrex, Inc.: 4 (https://510kreport.com/company/arthrex)
- Biomet, Inc.: 2 (https://510kreport.com/company/biomet)
- Bionx Implants, Inc.: 2 (https://510kreport.com/company/bionx-implants)
- Biomet Manufacturing Corp: 2 (https://510kreport.com/company/biomet-manufacturing)
- Linvatec Biomaterials, Ltd.: 1 (https://510kreport.com/company/linvatec-biomaterials)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)
- Stryker Leibinger GmbH & Co KG: 1 (https://510kreport.com/company/stryker-leibinger)

## Firms that cite its devices most
- Acumed, LLC: 1 (https://510kreport.com/company/acumed)

## Its most-cited devices
- K063244: Arc Surgical Bone Reduction Screw (2006), cited by 1

## Recent decisions
- K141559: V-Guide for Ventriculostomies (Feb 27, 2015)
- K071616: Arc Surgical Biotrak Pin System (Dec 19, 2007)
- K063244: Arc Surgical Bone Reduction Screw (Dec 27, 2006)
- K061763: Arc Surgical Biotrak Screw (Sep 19, 2006)
- K043176: Arc Surgical Resorbable Compression Screw System (Jun 17, 2005)

Source page: https://510kreport.com/company/arc-surgical