# Artoss GmbH

- Location (FDA's records): Rostock, DE
- FDA decisions: 3 (2015–2019): 3 510(k) clearances
- Product codes: MQV (3)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 2 (2 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
- Apatech, Ltd.: 3 (https://510kreport.com/company/apatech)
- Novabone Products, LLC: 2 (https://510kreport.com/company/novabone-products)

## Its most-cited devices
- K141189: Nanobone / Granulate (2015), cited by 1
- K161351: NanoBone SBX Putty (2016), cited by 1

## Recent decisions
- K190110: NanoBone SBX PUTTY, NanoBone QD (Apr 23, 2019)
- K161351: NanoBone SBX Putty (Oct 26, 2016)
- K141189: Nanobone / Granulate (Jan 30, 2015)

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