# Inmed Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 35 (1981–2003): 35 510(k) clearances
- Names in FDA's records: Inmed Corp. (32); Inmed Ltda. (3)
- Product codes: KNT (11), KOD (5), BTQ (2), CAE (2), KNQ (1), BTR (1), GYB (1), JXG (1), NWU (1), KGX (1), FWZ (1), BZW (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Parker Laboratories, Inc.: 2 (https://510kreport.com/company/parker-laboratories)
- American Heyer Schulte: 1 (https://510kreport.com/company/american-heyer-schulte)

## Firms that cite its devices most
- Rusch Intl.: 1 (https://510kreport.com/company/rusch-intl)

## Its most-cited devices
- K832672: Four Lumen Blakemore Tube (1983), cited by 1

## Recent decisions
- K030081: CSF400 and CSF600 (Oct 6, 2003)
- K030887: Lektrogel, Model LK3001 (Jun 13, 2003)
- K030889: Ultraekogel Models EK 2000 & EK 2001 (May 23, 2003)
- K862672: Esophageal Stethoscope with Thermistor (Oct 27, 1986)
- K853162: Sterile Nasopharyngeal Airway (Aug 6, 1985)
- K850152: Preconnected Urethral Catheter Tray (Mar 12, 1985)
- K850335: Ureteroscopy Catheter (Mar 12, 1985)
- K850248: Disposable Guedel Airway (Mar 12, 1985)

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