# Ivd Research, Inc.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 5 (2002–2009): 5 510(k) clearances
- Product codes: MHI (3), LLH (1), MHJ (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Meridian Diagnostics, Inc.: 1 (https://510kreport.com/company/meridian-diagnostics)
- Remel Co.: 1 (https://510kreport.com/company/remel)
- Lmd Laboratories: 1 (https://510kreport.com/company/lmd-laboratories)

## Recent decisions
- K081064: Giardia Fecal Antigen Detection Lateral Flow Kit, Model GL-LF (Jan 14, 2009)
- K032897: C. Difficile Toxin a + B Fecal Antigen Detection Microwell Elisa Kit Model; Cdiff-96 (May 27, 2004)
- K031059: Ivd Cryptosporidium Antigen Detection Assay, Model CP-96 (Jul 10, 2003)
- K024113: Ivd Crypto/Giardia Dfa (Mar 5, 2003)
- K020583: Ivd Giardia Antigen Detection Assay Model GL-96 (Sep 17, 2002)

Source page: https://510kreport.com/company/ivd-research