Altomed Limited
United KingdomFDA applicant, unverified
Part of Altomed Ltd
- Devices
- 1
What Altomed Limited makes
Altomed Limited manufactures Malhotra Platinum Segments, which are specialized ophthalmic surgical instruments.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry, with the company based in the United States.
Catalogue
Altomed Malhotra Platinum Segments Ref K170591
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Altomed Limited have in the registry?
The registry currently lists 1 device for Altomed Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Altomed Limited's devices?
Among its 1 most recently registered device, Altomed Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Altomed Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Altomed Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Altomed Limited in the registry?
The most recently registered devices listed for Altomed Limited include Altomed Malhotra Platinum Segments.