LEM Surgical AG
SwitzerlandFDA applicant, unverified FDA FEI 3040312029
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
Dynamis Robotic Surgical System Ref K260369
Regimes: 510(k) Registry: 510(k)Dynamis Robotic Surgical System Ref K243326
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3040312029
- DUNS number
- 480538984
- Address
- Morgenstrasse 136, Bern
- [email protected]
- Phone
- +1 (844) 684-9483
Frequently asked questions
How many devices does LEM Surgical AG have in the registry?
The registry currently lists 4 devices for LEM Surgical AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list LEM Surgical AG's devices?
Among its 4 most recently registered devices, LEM Surgical AG has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do LEM Surgical AG's devices fall under?
Among its 4 most recently registered devices, the classes recorded for LEM Surgical AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LEM Surgical AG in the registry?
The most recently registered devices listed for LEM Surgical AG include Dynamis Robotic Surgical System TPL0001, Dynamis Robotic Surgical System TPL0001-04 and Dynamis Robotic Surgical System.