# Rune Labs, Inc.

- Location (FDA's records): San Francisco, CA
- FDA decisions: 1 (2022–2022): 1 510(k) clearance
- Product codes: GYD (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- Gkc Manufacturing Pty, Ltd.: 1 (https://510kreport.com/company/gkc-manufacturing)

## Firms that cite its devices most
- H2o Bilisim Yazilim: 1 (https://510kreport.com/company/h2o-bilisim-yazilim)
- Nordic Kinetics AB: 1 (https://510kreport.com/company/nordic-kinetics)

## Its most-cited devices
- K213519: Rune Labs Tremor Transducer System (2022), cited by 2

## Recent decisions
- K213519: Rune Labs Tremor Transducer System (Jun 10, 2022)

Source page: https://510kreport.com/company/rune-labs