N.M. Beale Co., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 12
What N.M. Beale Co., Inc. makes
N.M. Beale Co., Inc. manufactures medical devices for procedural and endoscopic applications, including disposable ultrasonic endoscope balloons, scope introducers, and a water bottle designed for endoscopic use. Their portfolio also includes a powered exhalation filter (PEF) tube and a nebulizer system (EZ-MISTER) for respiratory therapy.
The company’s devices are classified as Class II under FDA regulations, with records supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does N.M. Beale Co., Inc. have in the registry?
The registry currently lists 12 devices for N.M. Beale Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list N.M. Beale Co., Inc.'s devices?
Among its 12 most recently registered devices, N.M. Beale Co., Inc. has devices listed in FDA 510(k) (5 devices) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do N.M. Beale Co., Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for N.M. Beale Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from N.M. Beale Co., Inc. in the registry?
The most recently registered devices listed for N.M. Beale Co., Inc. include N-Doe Pillow NDP, Ultramatrix EUS Radial Balloon for Olympus & Pentax USB-OR, Ultramatrix EUS Linear Balloon for Pentax USB-PL and Baleen Polyp Trap NBPT520.