# Azog, Inc.

- Location (FDA's records): Phillipsburg, NJ
- FDA decisions: 3 (2002–2004): 3 510(k) clearances
- Product codes: DHA (2), LCX (1)
- Predicates its devices cite: 2 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K022681: Azog, Inc. HCG One-Step Urine Pregnancy Test (Device or Cassette) (2002), cited by 1
- K022680: Azog, Inc. HCG One-Step Urine Pregnancy Test Strip (Dipstick) (2002), cited by 1

## Recent decisions
- K041748: Azog, Inc. HCG One-Step Urine Home Pregnancy Test (Dip Stick, Cassette and Midstream) (Aug 9, 2004)
- K022681: Azog, Inc. HCG One-Step Urine Pregnancy Test (Device or Cassette) (Nov 1, 2002)
- K022680: Azog, Inc. HCG One-Step Urine Pregnancy Test Strip (Dipstick) (Nov 1, 2002)

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