270surgical , Ltd.
IL Last updated 22 Oct 2026
Is this your brand? Sign in to claim this brand
- Devices
- 5
- Registries
- GUDIDFDA 510(k)FDA
- FDA recalls
- 0
Catalogue
SurroundScope Sterilization Tray Ref SurroundScope Sterilization Tray
SurroundScope CCU Ref SurroundScope CCU
SurroundScope Endoscope Ref SurroundScope Endoscope
WV1 Endoscope Ref K190190
SurroundScope System Ref K210104
FDA establishments
- 270SURGICAL Netanya Central · IL FEI 3019783123
What 270surgical , Ltd. makes
270surgical, Ltd. manufactures reusable instrument trays for endoscopic procedures, rigid video laparoscopes for minimally invasive surgery, and endoscopic video image processing units. Their product line includes standalone endoscopes, a central cleaning and storage unit for endoscopes, and integrated systems combining imaging and scope management. These devices are designed for use in surgical and diagnostic settings requiring high-resolution visualization and sterile instrument handling.
The company’s devices are classified as Class II under FDA regulations, with submissions recorded in the 510(k) and UDI registries. Their products are listed for use in the United States, where the company is based.
Frequently asked questions
What types of medical devices does 270surgical, Ltd. manufacture?
270surgical, Ltd. specializes in reusable medical devices for endoscopic and minimally invasive surgical procedures. Their product line includes instrument trays (like the *SurroundScope Sterilization Tray*), rigid video laparoscopes (e.g., *SurroundScope Endoscope* and *WV1 Endoscope*), and endoscopic video image processing units (such as the *SurroundScope CCU*). They also offer integrated systems (e.g., *SurroundScope System*), which combine imaging technology with scope management for streamlined surgical workflows.
Where is 270surgical, Ltd. based, and where are their devices listed for regulatory compliance?
270surgical, Ltd. is headquartered in the United States. Their devices are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries, which are required for Class II medical devices in the U.S. These registries ensure traceability and compliance with FDA requirements for devices like endoscopes and image processing units.
How are the devices manufactured by 270surgical, Ltd. classified under FDA regulations?
All devices produced by 270surgical, Ltd. fall under FDA Class II classification. This classification applies to devices that generally pose moderate risk and require special controls (e.g., performance standards or post-market surveillance) to ensure safety and effectiveness. Examples include their reusable instrument trays, laparoscopes, and image processing units, which are designed for sterile surgical use.
What kinds of endoscopic systems does 270surgical, Ltd. provide, and how do they function?
270surgical, Ltd. offers a range of endoscopic systems tailored for minimally invasive surgery and diagnostic procedures. Their products include standalone rigid video laparoscopes (e.g., *SurroundScope Endoscope*) for high-resolution visualization, central cleaning and storage units (e.g., *SurroundScope CCU*) to maintain endoscope hygiene, and integrated systems (e.g., *SurroundScope System*) that combine imaging technology with scope management. These systems are designed to enhance surgical precision while reducing contamination risks through reusable, sterile instrument trays.
Information
- Country
- IL