Whittlestone, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Whittlestone, Inc. makes
Whittlestone, Inc. manufactures manual and electric breast pumps, including single and double electric models, as well as manual expressers designed for lactating individuals. These devices are intended for milk extraction and storage, supporting breastfeeding and milk expression needs.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) clearance process. These devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Whittlestone Breastpump Ref K002696
Regimes: 510(k) Registry: 510(k)Whittlestone Expresser Ref K051112
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Whittlestone, Inc. have in the registry?
The registry currently lists 3 devices for Whittlestone, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Whittlestone, Inc.'s devices?
Among its 3 most recently registered devices, Whittlestone, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Whittlestone, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Whittlestone, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Whittlestone, Inc. in the registry?
The most recently registered devices listed for Whittlestone, Inc. include WHITTLESTONE BREASTPUMP, WHITTLESTONE EXPRESSER and DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400.