# Radius Intl., Inc.

- Location (FDA's records): Tarpon Springs, FL
- FDA decisions: 5 (1995–1998): 5 510(k) clearances
- Product codes: KNT (3), IOR (1), BSS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 29 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- C.R. Bard, Inc.: 2 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K972025: Radius Pull Percutaneous Endoscopic Gastrostomy Kit (1998), cited by 1
- K972102: Radius Push Over the Guide Wire Percutaneous Endoscopic Gastrostomy Kit (1998), cited by 1

## Recent decisions
- K972025: Radius Pull Percutaneous Endoscopic Gastrostomy Kit (Jan 23, 1998)
- K972102: Radius Push Over the Guide Wire Percutaneous Endoscopic Gastrostomy Kit (Jan 23, 1998)
- K971901: Radius Low Profile Gastrostomy Tube Kit (Jan 22, 1998)
- K951560: Radius Manual Whwwlchairs (Cobra, Viper, Swing, Olympia, and Mobil Models) (Apr 17, 1995)
- K930510: Radius Enteral Feeding Tube (Feb 1, 1995)

Source page: https://510kreport.com/company/radius-intl