Penner Manufacturing, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Penner Manufacturing, Inc. makes
Penner Manufacturing, Inc. produces height-adjustable bath systems, including models like the Pacific Recumbent, Superior Bath (Model 6300), and Cascade Bath (Model 6900). These devices are designed for adjustable water depth and user positioning to support bathing assistance.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The portfolio is regulated in the United States.
Catalogue
Pacific Recumbent Height-Adjustable Bath System Ref K040772
Regimes: 510(k) Registry: 510(k)Superior Bath, Model 6300 Ref K012061
Regimes: 510(k) Registry: 510(k)Cascade Bath, Model 6900 Ref K012057
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Penner Manufacturing, Inc. have in the registry?
The registry currently lists 3 devices for Penner Manufacturing, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Penner Manufacturing, Inc.'s devices?
Among its 3 most recently registered devices, Penner Manufacturing, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Penner Manufacturing, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Penner Manufacturing, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Penner Manufacturing, Inc. in the registry?
The most recently registered devices listed for Penner Manufacturing, Inc. include PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEM, SUPERIOR BATH, MODEL 6300 and CASCADE BATH, MODEL 6900.