# Biowy Corporation

- Location (FDA's records): Lake Forest, CA
- FDA decisions: 3 (2018–2024): 3 510(k) clearances
- Product codes: LJS (2), ETD (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 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
- Micromedics, Inc.: 1 (https://510kreport.com/company/micromedics)
- Bard Access Systems, Inc.: 1 (https://510kreport.com/company/bard-access-systems)

## Its most-cited devices
- K173956: Biowy PlCC Catheter (2018), cited by 1

## Recent decisions
- K233658: Biowy Tym Tube (TT) (Feb 16, 2024)
- K192246: Biowy PICC Catheter S Kit (Apr 30, 2020)
- K173956: Biowy PlCC Catheter (May 21, 2018)

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