# Tautona Group, LLC

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 2 (2013–2024): 2 510(k) clearances
- Names in FDA's records: Tautona Group, LLC (1); Tautona Group (1)
- Product codes: FMF (1), HIF (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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
- Nordson Efd: 1 (https://510kreport.com/company/nordson-efd)
- Shippert Medical Technologies Corp.: 1 (https://510kreport.com/company/shippert-medical-technologies)
- Tautona Group Research & Development, Co., LLC: 1 (https://510kreport.com/company/tautona-group-research-development)

## Recent decisions
- K242536: TauTona Pneumoperitoneum Assist Device (TPAD) (Oct 15, 2024)
- K131963: Tautona Injector Device (Oct 22, 2013)

Source page: https://510kreport.com/company/tautona-group