# Hoogland Spine Products, GmbH

- Location (FDA's records): Muenchen, DE
- FDA decisions: 3 (2009–2022): 3 510(k) clearances
- Product codes: HRX (2), GEI (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Joimax GmbH: 3 (https://510kreport.com/company/joimax)
- Richard Wolf Medical Instruments Corp.: 2 (https://510kreport.com/company/richard-wolf-medical-instruments)
- Arthro Kinetics, Inc.: 2 (https://510kreport.com/company/arthro-kinetics)

## Firms that cite its devices most
- Asap Endoscopic Products GmbH: 1 (https://510kreport.com/company/asap-endoscopic-products)
- Theken Spine, LLC: 1 (https://510kreport.com/company/theken-spine)
- Biovision Technologies, LLC: 1 (https://510kreport.com/company/biovision-technologies)

## Its most-cited devices
- K083552: Maxmorespine Tom Stick (2009), cited by 2
- K090132: Maxmorespine Spinal System (2009), cited by 1

## Recent decisions
- K211173: maxmorespine Bipolar Electrodes (Jun 23, 2022)
- K083552: Maxmorespine Tom Stick (Oct 9, 2009)
- K090132: Maxmorespine Spinal System (Jun 9, 2009)

Source page: https://510kreport.com/company/hoogland-spine-products