# Lode Corp.

- Location (FDA's records): Seattle, WA
- FDA decisions: 3 (1985–2020): 3 510(k) clearances
- Names in FDA's records: Lode Corp. (2); Lode B.V. (1)
- Product codes: ISD (2), JPA (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Electromed, Inc.: 1 (https://510kreport.com/company/electromed)
- Ergoline GmbH: 1 (https://510kreport.com/company/ergoline)

## Its most-cited devices
- K851097: Lode Model Corival Ergometer (1985), cited by 2

## Recent decisions
- K202979: MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal Ultra (Dec 21, 2020)
- K852450: Lode Coagulometer Model LC-6 (Sep 30, 1985)
- K851097: Lode Model Corival Ergometer (Jun 18, 1985)

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