Dutton-Lainson Co.
Country not established
- Devices
- 3
What Dutton-Lainson Co. makes
Dutton-Lainson Co. manufactures mobility and patient care devices, including the Sanitas Patient Lift for safe patient transfer, the Sanitas Whirlpool Bathing System for therapeutic bathing, and the Sanitas Patient Scale for clinical weight measurement.
These products are regulated under the FDA’s 510(k) pathway, with some classified as Class I and others as Class II. The company’s devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Sanitas Patient Lift Ref K930625
510(k) 510(k)Sanitas Whirpool Bathing System Ref K930624
510(k) 510(k)Sanitas Patient Scale Ref K930626
510(k) 510(k)
Frequently asked questions
How many devices does Dutton-Lainson Co. have in the registry?
The registry currently lists 3 devices for Dutton-Lainson Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dutton-Lainson Co.'s devices?
Among its 3 most recently registered devices, Dutton-Lainson Co. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dutton-Lainson Co.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dutton-Lainson Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dutton-Lainson Co. in the registry?
The most recently registered devices listed for Dutton-Lainson Co. include SANITAS PATIENT LIFT, SANITAS WHIRPOOL BATHING SYSTEM and SANITAS PATIENT SCALE.