Zygotek Assoc.
United KingdomFDA 510(k) applicant, unverified
- Devices
- 1
What Zygotek Assoc. makes
Zygotek Assoc. manufactures the FlexiStand Major, a medical device designed for patient positioning and support, likely used in clinical or home care settings to assist with mobility or stability during procedures or daily activities.
The FlexiStand Major is classified under FDA’s 510(k) pathway, indicating it is regulated as a Class II medical device in the United States. The company is based in the US.
Catalogue
Flexistand Major Ref K852152
510(k) 510(k)
Frequently asked questions
How many devices does Zygotek Assoc. have in the registry?
The registry currently lists 1 device for Zygotek Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zygotek Assoc.'s devices?
Among its 1 most recently registered device, Zygotek Assoc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Zygotek Assoc. in the registry?
The most recently registered devices listed for Zygotek Assoc. include FLEXISTAND MAJOR.