T. Korossurgical Instruments Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 27
What T. Korossurgical Instruments Corp. makes
T. Korossurgical Instruments Corp. manufactures reusable and single-use surgical instruments for orthopedic, arthroscopic, and cardiovascular procedures, including retractors for cervical and sternal applications, endoscopic tools like scissors and graspers, and meniscal cutters. Their portfolio also includes irrigation-equipped videoscope systems, sutures for sternotomy, and vascular clamps designed for precision in minimally invasive and open surgeries.
The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Products are listed in the FDA’s 510(k) registry, reflecting their regulatory pathway in the United States.
Catalogue
Search and filter all 27 devicesFrequently asked questions
How many devices does T. Korossurgical Instruments Corp. have in the registry?
The registry currently lists 27 devices for T. Korossurgical Instruments Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list T. Korossurgical Instruments Corp.'s devices?
Among its 27 most recently registered devices, T. Korossurgical Instruments Corp. has devices listed in FDA 510(k) (27 devices).
What risk classes do T. Korossurgical Instruments Corp.'s devices fall under?
Among its 27 most recently registered devices, the classes recorded for T. Korossurgical Instruments Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from T. Korossurgical Instruments Corp. in the registry?
The most recently registered devices listed for T. Korossurgical Instruments Corp. include CERVICAL SELF-RETAINING RETRACTOR, STERNUM SPREADER AND MITRAL VALVE RETRACTOR, PERCUTANEOUS DISCECTOMY CANNULA SYSTEM and STERNUM SPREADER, PEDIATRIC.