Schoelly Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Schoelly Technologies, Inc. makes
Schoelly Technologies, Inc. manufactures rod-lens viewing and operating laparoscopes, which are used for minimally invasive abdominal and pelvic surgeries, as well as rigid rod-lens arthroscopes for diagnostic joint examinations. These devices enable visualisation and manipulation of internal tissues through small incisions, supporting procedures in orthopaedics and general surgery.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, reflecting their compliance with US regulatory requirements. The company is headquartered in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Arthroscope, Rigid Rod-Lens Diagnostic Endoscope Ref K943426
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schoelly Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Schoelly Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schoelly Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Schoelly Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Schoelly Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Schoelly Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schoelly Technologies, Inc. in the registry?
The most recently registered devices listed for Schoelly Technologies, Inc. include LAPAROSCOPE, ROD-LENS VIEWING AND OPERATING ENDOSCOPE and ARTHROSCOPE, RIGID ROD-LENS DIAGNOSTIC ENDOSCOPE.