Altomec Endoscopy, Inc.
Country not established
- Devices
- 1
What Altomec Endoscopy, Inc. makes
Altomec Endoscopy, Inc. manufactures arthroscopes, which are minimally invasive surgical instruments used for visualizing, diagnosing, and treating joint conditions within the knee, shoulder, and other articulations. These devices feature high-definition optics and ergonomic handles to enhance precision during arthroscopic procedures, supporting procedures like meniscus repair, ligament reconstruction, and synovial tissue evaluation.
The company’s arthroscopes are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) database, adhering to U.S. regulatory standards for surgical endoscopy tools. The manufacturer operates from the United States.
Catalogue
Altomec Arthroscope Ref K112548
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Altomec Endoscopy, Inc. have in the registry?
The registry currently lists 1 device for Altomec Endoscopy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Altomec Endoscopy, Inc.'s devices?
Among its 1 most recently registered device, Altomec Endoscopy, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Altomec Endoscopy, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Altomec Endoscopy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Altomec Endoscopy, Inc. in the registry?
The most recently registered devices listed for Altomec Endoscopy, Inc. include ALTOMEC ARTHROSCOPE.