Origin Medsystems, Inc.
United StatesFDA applicant, unverified
- Devices
- 50
What Origin Medsystems, Inc. makes
Origin Medsystems, Inc. manufactures single-use surgical instruments and devices for minimally invasive procedures, including distension balloons for laparoscopic and arthroscopic applications, laparoscopic retractors, and trocar systems with sensing tips. Their portfolio also includes cement extraction kits, ligator devices, hook instruments, and preperitoneal balloon systems for specific surgical modifications. These products are designed for use in orthopedic, orthopedic trauma, and general surgical procedures.
The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. Their instruments are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Search and filter all 50 devicesFrequently asked questions
How many devices does Origin Medsystems, Inc. have in the registry?
The registry currently lists 50 devices for Origin Medsystems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Origin Medsystems, Inc.'s devices?
Among its 50 most recently registered devices, Origin Medsystems, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Origin Medsystems, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Origin Medsystems, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Origin Medsystems, Inc. in the registry?
The most recently registered devices listed for Origin Medsystems, Inc. include DISTENTION BALLOON, LAPAROSCOPIC BALLOON RETRACTOR, PSB PREPERITONEAL STRUCTURE BALLOON and SENSING TIP SURGICAL TROCAR.