# Acromed Corp.

- Location (FDA's records): Cleveland, OH
- FDA decisions: 41 (1984–1998): 41 510(k) clearances
- Product codes: MNH (14), KWP (14), KWQ (11), MNI (1)
- Predicates its devices cite: 15 (15 its own); citations of its devices by later devices: 87 (15 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medos International SARL: 28 (https://510kreport.com/company/medos-international)
- Depuy Spine, Inc.: 5 (https://510kreport.com/company/depuy-spine)
- Depuyacromed: 4 (https://510kreport.com/company/depuyacromed)
- Depuy, Inc.: 4 (https://510kreport.com/company/depuy)
- Scien'Tx USA, Inc.: 2 (https://510kreport.com/company/scien-tx-usa)
- K2m, Inc.: 2 (https://510kreport.com/company/k2m)
- Biomet Spine (Aka Ebi, LLC): 2 (https://510kreport.com/company/biomet-spine-aka-ebi)
- Advanced Medical Technologies AG: 2 (https://510kreport.com/company/advanced-medical-technologies)

## Its most-cited devices
- K980485: Isola Spinal System (1998), cited by 14
- K971248: Kaneda SR Anterior Spinal System (1997), cited by 7
- K974757: Kaneda Anterior Scoliosis System Kass (1998), cited by 7
- K962984: Isola Pediatric Components (1996), cited by 5
- K972718: M-2 Anterior Plate System (1997), cited by 5
- K952236: Isola System (1996), cited by 5

## Recent decisions
- K980485: Isola Spinal System (Oct 21, 1998)
- K981714: Timx Low Back System Titanium MX Rod Based Low Back System (Jun 30, 1998)
- K981113: Pediatric PRC (May 29, 1998)
- K981274: Acromed Timx Plate Based Low Back System (Apr 29, 1998)
- K980228: University Plate Anterior System (Apr 14, 1998)
- K974757: Kaneda Anterior Scoliosis System Kass (Mar 5, 1998)
- K972718: M-2 Anterior Plate System (Oct 1, 1997)
- K970955: Acromed Anterior Cervical Stabilization System (Jun 11, 1997)

Source page: https://510kreport.com/company/acromed
