The Altomec Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What The Altomec Corp. makes
The Altomec Corp. manufactures surgical trocar systems and telescopes with integrated working channels, designed for minimally invasive procedures such as single-port endoscopic surgeries (SEPS). These devices are intended for use in laparoscopic and endoscopic applications where precise access and visualization are required.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Etb Trocar System Ref K990894
Regimes: 510(k) Registry: 510(k)Etb Telescope W/Working Channel For Seps Ref K972298
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Altomec Corp. have in the registry?
The registry currently lists 2 devices for The Altomec Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Altomec Corp.'s devices?
Among its 2 most recently registered devices, The Altomec Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do The Altomec Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Altomec Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Altomec Corp. in the registry?
The most recently registered devices listed for The Altomec Corp. include ETB TROCAR SYSTEM and ETB TELESCOPE W/WORKING CHANNEL FOR SEPS.