# Paragon Bioteck, Inc.

- Location (FDA's records): Portland, OR
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: LZU (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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
- Lacrimedics, Inc.: 1 (https://510kreport.com/company/lacrimedics)
- Eagle Vision, Inc.: 1 (https://510kreport.com/company/eagle-vision)

## Firms that cite its devices most
- Riverpoint Medical: 1 (https://510kreport.com/company/riverpoint-medical)

## Its most-cited devices
- K140711: Comfortear Lacrisolve Absorbable Punctum Plug, Lacrisolve Absorbable Punctum Plug, Comfortear Lacrisolve Punctum Plug, (2014), cited by 1

## Recent decisions
- K140711: Comfortear Lacrisolve Absorbable Punctum Plug, Lacrisolve Absorbable Punctum Plug, Comfortear Lacrisolve Punctum Plug, (Jun 20, 2014)

Source page: https://510kreport.com/company/paragon-bioteck