Dawn Medical
Country not established
- Devices
- 4
What Dawn Medical makes
Dawn Medical manufactures respiratory monitoring systems, including the Somnigauge thoracic/abdominal expansion monitoring system and the Somniprobe II nasal and buccal airflow monitoring system. The company also produces a closed drainage system for seromas, the Seroma-Cath, and disposable biopsy forceps for medical procedures.
These devices are classified as Class I and Class II under FDA regulations, with some models requiring 510(k) clearance. The company is based in the United States and its products are listed in the FDA’s 510(k) registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Seroma-Cath Close Drainage System Ref K905733
Regimes: 510(k) Registry: 510(k)Dawn Disposable Biopsy Forceps Ref K933135
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dawn Medical have in the registry?
The registry currently lists 4 devices for Dawn Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dawn Medical's devices?
Among its 4 most recently registered devices, Dawn Medical has devices listed in FDA 510(k) (4 devices).
What risk classes do Dawn Medical's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Dawn Medical's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dawn Medical in the registry?
The most recently registered devices listed for Dawn Medical include SOMNIGAUGE THORACIC/ABDOMINAL EXPANSION MON. SYST., SOMNIPROBE II NASAL AND BUCCAL AIRFLOW MON. SYST., SEROMA-CATH CLOSE DRAINAGE SYSTEM and DAWN DISPOSABLE BIOPSY FORCEPS.