# Innerdyne Medical, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 6 (1993–1994): 6 510(k) clearances
- Product codes: GCJ (5), DYB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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
- Innerdyne, Inc.: 7 (https://510kreport.com/company/innerdyne)

## Its most-cited devices
- K940232: Innerdyne Step Trocar Expandable Port, S.T.E.P. (1994), cited by 3
- K943253: Innerdyne Step Trocar Expandable Port, S.T.E.P. (1994), cited by 3
- K931489: Intherm Radially Expanding Dilating Introducer (1993), cited by 1

## Recent decisions
- K943253: Innerdyne Step Trocar Expandable Port, S.T.E.P. (Oct 11, 1994)
- K943056: Single Stick Radially Expanding Dilator (Sep 27, 1994)
- K940428: Innerdyne Single-Stick Radially Expanding Dilator (Apr 25, 1994)
- K940232: Innerdyne Step Trocar Expandable Port, S.T.E.P. (Apr 18, 1994)
- K932692: Innerdyne Medical Laparoscopic Sphincterotomy Kit (Dec 27, 1993)
- K931489: Intherm Radially Expanding Dilating Introducer (Oct 15, 1993)

Source page: https://510kreport.com/company/innerdyne-medical
