# Tusker Medical, Inc.

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 3 (2017–2026): 2 510(k) clearances and 1 original PMA approval
- Names in FDA's records: Tusker Medical, Inc. (2); Tusker Medical (1)
- Product codes: ETD (2), QJA (1)
- Predicates its devices cite: 2 (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
- Acclarent, Inc.: 1 (https://510kreport.com/company/acclarent)
- Preceptis Medical: 1 (https://510kreport.com/company/preceptis-medical)

## Recent decisions
- K252436: Tula Tympanostomy Tube Delivery Device (Apr 23, 2026)
- P190016: Tula® System (Nov 25, 2019)
- K171239: TULA Tube Delivery System (Jun 28, 2017)

Source page: https://510kreport.com/company/tusker-medical