# Aardvark Medical, Inc.

- Location (FDA's records): Ross, CA
- FDA decisions: 2 (2008–2023): 2 510(k) clearances
- Names in FDA's records: Aardvark Medical, Inc. (1); Aardvark Medical (1)
- Product codes: QBD (1), JCX (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (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
- Longhorn Vaccines and Diagnostics, LLC: 1 (https://510kreport.com/company/longhorn-vaccines-and-diagnostics)
- Respironics, Inc.: 1 (https://510kreport.com/company/respironics)
- Sunrise Medical Hhg, Inc.: 1 (https://510kreport.com/company/sunrise-medical-hhg)
- Emg Technology Co., Ltd.: 1 (https://510kreport.com/company/emg-technology)

## Firms that cite its devices most
- Avita Corporation: 1 (https://510kreport.com/company/avita)
- Hospitech Respiration, Ltd.: 1 (https://510kreport.com/company/hospitech-respiration)

## Its most-cited devices
- K082762: Aardvark Nasal Irrigation and Aspiration Device (2008), cited by 2

## Recent decisions
- K221664: CLEARinse CTS Specimen Collection and Transport System (Jul 3, 2023)
- K082762: Aardvark Nasal Irrigation and Aspiration Device (Nov 12, 2008)

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