Olympus Surgical Technologies America
Country not established
- Devices
- 14
What Olympus Surgical Technologies America makes
The company manufactures endoscopic imaging systems, including flexible laparoscopes like the ViziShot 2 FLEX, and hemostasis tools such as the Gyrus ACMI Bicoag Hemostasis Probe. It also produces ureteral dilation catheters (e.g., Uro-EZDilate and EZDilate 3-Stage Balloon Dilatation Catheter), surgical sealers and dividers (e.g., PowerSeal Curved Jaw Sealer), laser systems (SOLTIVE Pro/Premium SuperPulsed Laser and associated fibers), and accessories like the CleverLock Guidewire Locking Device and PeriView FLEX imaging probes. Variable-length access sheaths (VARI-PASS) are part of its portfolio as well.
All listed devices fall under Class II regulatory classification in the US and are recorded in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Search and filter all 14 devicesFrequently asked questions
How many devices does Olympus Surgical Technologies America have in the registry?
The registry currently lists 14 devices for Olympus Surgical Technologies America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Olympus Surgical Technologies America's devices?
Among its 14 most recently registered devices, Olympus Surgical Technologies America has devices listed in FDA 510(k) (14 devices).
What risk classes do Olympus Surgical Technologies America's devices fall under?
Among its 14 most recently registered devices, the classes recorded for Olympus Surgical Technologies America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Olympus Surgical Technologies America in the registry?
The most recently registered devices listed for Olympus Surgical Technologies America include SOLTIVE™ Laser System (SOLTIVE™ Pro SuperPulsed Laser), ViziShot 2 FLEX, GYRUS ACMI BICOAG HEMOSTASIS PROBE and POWERSEAL Curved Jaw Sealer and Divider, Double Action.