Theotclab Healthcare B.V.
NetherlandsFDA applicant, unverified FDA FEI 3020164048
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dr. Yglo Wart Remover Ref K210529
Regimes: 510(k) Registry: 510(k)Dr. Yglo Skin Tag Remover Ref K251524
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3020164048
- Address
- Fred. Roeskestraat 115, Amsterdam Noord-Holland
Frequently asked questions
How many devices does Theotclab Healthcare B.V. have in the registry?
The registry currently lists 2 devices for Theotclab Healthcare B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Theotclab Healthcare B.V.'s devices?
Among its 2 most recently registered devices, Theotclab Healthcare B.V. has devices listed in FDA 510(k) (2 devices).
What risk classes do Theotclab Healthcare B.V.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Theotclab Healthcare B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Theotclab Healthcare B.V. in the registry?
The most recently registered devices listed for Theotclab Healthcare B.V. include Dr. Yglo Wart Remover and Dr. Yglo Skin Tag Remover.