# Crossbay Medical, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 6 (2014–2020): 6 510(k) clearances
- Names in FDA's records: Crossbay Medical, Inc. (3); Crossbay Medical (3)
- Product codes: HHK (2), MQF (1), LKF (1), PGK (1), PON (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 1 (1 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
- Femasys, Inc.: 2 (https://510kreport.com/company/femasys)
- Cook Urological, Inc.: 2 (https://510kreport.com/company/cook-urological)
- Portex, Inc.: 1 (https://510kreport.com/company/portex)
- Marina Medical Instruments, Inc.: 1 (https://510kreport.com/company/marina-medical-instruments)
- Gtimd, LLC: 1 (https://510kreport.com/company/gtimd)

## Its most-cited devices
- K192534: CrossBay Endometrial Tissue Sampler (ETS) (2020), cited by 1

## Recent decisions
- K201952: CrossGlide ETS Plus (Aug 5, 2020)
- K192534: CrossBay Endometrial Tissue Sampler (ETS) (Mar 25, 2020)
- K190813: CrossBay Cervical Dilator Catheter System (Aug 23, 2019)
- K162064: CrossBay IVF Embryo Transfer Catheter Set (Jan 5, 2017)
- K142545: SonoFlow Sonohysterography and Sonohysterosalpingography Device (Mar 20, 2015)
- K133144: Sonosure Sonohysterography & Endometrial Sampling Device (Mar 19, 2014)

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