# Portlyn Corp.

- Location (FDA's records): Moultonboro, NH
- FDA decisions: 8 (1990–1997): 8 510(k) clearances
- Product codes: FCL (2), DWZ (2), HET (2), EOQ (1), KGE (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Curon Medical, Inc.: 1 (https://510kreport.com/company/curon-medical)

## Its most-cited devices
- K970083: Dynabite Hot GI Biopsy Forceps (1997), cited by 1

## Recent decisions
- K970083: Dynabite Hot GI Biopsy Forceps (Jun 17, 1997)
- K951447: Dynabite Cardiovascular Biopsy Forceps (Jul 27, 1995)
- K952391: Dynabite Urological Forceps (Jun 1, 1995)
- K944245: Dynabite Laparoscopic Forceps (Nov 15, 1994)
- K934506: Dynabite Hysteroscopic Forceps (Mar 22, 1994)
- K901300: Biopsy Forceps (Jun 29, 1990)
- K896147: Biopsy Forcep (Non-Electric) (Apr 16, 1990)
- K896146: Biopsy Forceps, (Non-Rigid) (Mar 9, 1990)

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