# Fidia Pharmaceutical Corp.

- Location (FDA's records): Washington, DC
- FDA decisions: 10 (1997–1999): 10 510(k) clearances
- Product codes: MGQ (10)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 8 (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
- Telios Pharmaceuticals, Inc.: 2 (https://510kreport.com/company/telios-pharmaceuticals)
- Carrington Laboratories, Inc.: 2 (https://510kreport.com/company/carrington-laboratories)
- Convatec, A Division of E.R. Squibb & Sons: 2 (https://510kreport.com/company/convatec-a-division-of-er-squibb-sons)

## Firms that cite its devices most
- Synedgen, Inc.: 2 (https://510kreport.com/company/synedgen)
- Glycobiosciences, Inc.: 2 (https://510kreport.com/company/glycobiosciences)
- Kytogenics, Inc.: 1 (https://510kreport.com/company/kytogenics)
- L.A.M. Pharmaceutical, Corp.: 1 (https://510kreport.com/company/lam-pharmaceutical)
- Virchow Biotech Pvt, Ltd.: 1 (https://510kreport.com/company/virchow-biotech-pvt)

## Its most-cited devices
- K984413: Bionect Hydrogel (1999), cited by 3
- K963004: Bionect Cream (1997), cited by 2
- K984264: Modification of Bionect Clear Hydrogel (1999), cited by 2
- K973725: Bionect Clear Hydrogel (1998), cited by 1

## Recent decisions
- K984267: Modification of Bionect Hydrogel Foam (Feb 10, 1999)
- K984266: Modification of Bionect Hydrogel Spray (Feb 10, 1999)
- K984262: Modification of Bionect Hydrogel Gauze Pads (Feb 10, 1999)
- K984413: Bionect Hydrogel (Feb 10, 1999)
- K984264: Modification of Bionect Clear Hydrogel (Feb 10, 1999)
- K973725: Bionect Clear Hydrogel (Sep 22, 1998)
- K973722: Bionect Hydrogel Foam (Sep 22, 1998)
- K973724: Bionect Hydrogel Spray (Sep 22, 1998)

Source page: https://510kreport.com/company/fidia-pharmaceutical