# Sparo, Inc.

- Location (FDA's records): Saint Louis, MO
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: BZH (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (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
- Microlife Intellectual Property GmbH: 1 (https://510kreport.com/company/microlife-intellectual-property)

## Firms that cite its devices most
- Breathe Me, Ltd.: 1 (https://510kreport.com/company/breathe-me)
- Multisensor Diagnostics (Dba Aidar Health): 1 (https://510kreport.com/company/multisensor-diagnostics-dba-aidar-health)
- Knox Medical Diagnostics: 1 (https://510kreport.com/company/knox-medical-diagnostics)

## Its most-cited devices
- K152276: Wing Smart FEVI and Peak Flow Meter (2016), cited by 3

## Recent decisions
- K152276: Wing Smart FEVI and Peak Flow Meter (Jun 3, 2016)

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