# Trutek, Inc.

- Location (FDA's records): Crofton, MD
- FDA decisions: 2 (2003–2006): 2 510(k) clearances
- Names in FDA's records: Trutek, Inc. (1); Trutek Corp (1)
- Product codes: FLL (1), NUP (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
- Dr. Theiss Naturwaren GmbH: 1 (https://510kreport.com/company/dr-theiss-naturwaren)

## Firms that cite its devices most
- Hi-Tech Pharmacal, Inc.: 1 (https://510kreport.com/company/hi-tech-pharmacal)
- Haymax Limited: 1 (https://510kreport.com/company/haymax)

## Its most-cited devices
- K053625: Nasalguard (2006), cited by 2

## Recent decisions
- K053625: Nasalguard (Feb 22, 2006)
- K023510: Trutek Select Model TT-1001 (Feb 4, 2003)

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