# Acra Cut, Inc.

- Location (FDA's records): Acton, MA
- FDA decisions: 8 (1983–2003): 8 510(k) clearances
- Product codes: HBF (3), HBE (2), HAO (2), HBO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- The Anspach Effort, Inc.: 2 (https://510kreport.com/company/anspach-effort)
- Emd Endoszkop Muszer Gyarto ES Kereskedelmi Kft.: 1 (https://510kreport.com/company/emd-endoszkop-muszer-gyarto-es-kereskedelmi-kft)
- Codman & Shurtleff, Inc.: 1 (https://510kreport.com/company/codman-shurtleff)
- Micromar Ind. Com., Ltd.: 1 (https://510kreport.com/company/micromar-ind-com)
- Adeor Medical Technologies GmbH: 1 (https://510kreport.com/company/adeor-medical-technologies)
- Evonos GmbH & Co. KG: 1 (https://510kreport.com/company/evonos)
- Stryker Ireland Ltd., Instruments Division: 1 (https://510kreport.com/company/stryker-ireland-instruments-division)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)

## Its most-cited devices
- K892866: Automatic Cranial Drill (Perforator) (1989), cited by 4
- K833266: Acra-Cut (1983), cited by 4
- K944311: Acra-Cut (1994), cited by 1

## Recent decisions
- K032970: Acra-Cut Xpress 120 (Dec 8, 2003)
- K944311: Acra-Cut (Nov 18, 1994)
- K911812: Acra-Cut Wire Pass Drill (Sep 10, 1991)
- K911819: Acra-Cut Neurological Surgical Device-Powered (Sep 10, 1991)
- K910225: Bone Pad Remover (Feb 12, 1991)
- K910226: Dural Dissectors (Feb 12, 1991)
- K892866: Automatic Cranial Drill (Perforator) (Jun 15, 1989)
- K833266: Acra-Cut (Dec 29, 1983)

Source page: https://510kreport.com/company/acra-cut