# Zephyr Technology Corporation

- Location (FDA's records): Stamford, CT
- FDA decisions: 4 (2010–2013): 4 510(k) clearances
- Product codes: MHX (2), DRX (1), DRG (1)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 6 (2 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
- Monebo Technologies, Inc.: 1 (https://510kreport.com/company/monebo-technologies)
- Hidalgo Limited: 1 (https://510kreport.com/company/hidalgo)
- Respironics, Inc.: 1 (https://510kreport.com/company/respironics)
- Vivometrics, Inc.: 1 (https://510kreport.com/company/vivometrics)
- Gmp/Companies, Inc.: 1 (https://510kreport.com/company/gmp-companies)

## Firms that cite its devices most
- Nimbleheart, Inc.: 1 (https://510kreport.com/company/nimbleheart)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)
- Connected Sensing- A Division of Philips Medical Systems: 1 (https://510kreport.com/company/connected-sensing-a-division-of-philips-medical-systems)
- Rooti Labs, Ltd.: 1 (https://510kreport.com/company/rooti-labs)

## Its most-cited devices
- K123658: Biomodule 3-M1 (2013), cited by 3
- K113045: Bioharness (2012), cited by 2
- K100040: Bioharness (2010), cited by 1

## Recent decisions
- K122763: Physiological Data Processor (Jun 20, 2013)
- K123658: Biomodule 3-M1 (Apr 24, 2013)
- K113045: Bioharness (Aug 14, 2012)
- K100040: Bioharness (Dec 3, 2010)

Source page: https://510kreport.com/company/zephyr-technology