# Drg Intl., Inc.

- Location (FDA's records): East Stroudsburg, PA
- FDA decisions: 4 (2000–2008): 4 510(k) clearances
- Product codes: CDZ (2), JLX (1), NHG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K062534: Enzyme Immunoassay for the Detection of Salivary 17-a-Hydroxyprogesterone (Jan 29, 2008)
- K052649: DRG SLV Testosterone Elisa Test (Jan 27, 2006)
- K051733: Enzyme Immunoassay for the Detection of Salivary Cortisol (Dec 7, 2005)
- K000043: DRG Aurica Elisa Testosterone Kit (Apr 17, 2000)

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