Sightline Technologies, Ltd.
IsraelFDA applicant, unverified
- Devices
- 3
What Sightline Technologies, Ltd. makes
Sightline Technologies, Ltd. manufactures endoscopic imaging devices, including the RECTOSIGHT RS300-04 and PROTOSIGHT PS300-04 for rectal and protoscopic examinations, as well as the COLONOSIGHT Model 510B for colonoscopy procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Rectosight Rs 300-04 Ref K994130
Regimes: 510(k) Registry: 510(k)Colonosight Model 510B Ref K032688
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sightline Technologies, Ltd. have in the registry?
The registry currently lists 3 devices for Sightline Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sightline Technologies, Ltd.'s devices?
Among its 3 most recently registered devices, Sightline Technologies, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Sightline Technologies, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sightline Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sightline Technologies, Ltd. in the registry?
The most recently registered devices listed for Sightline Technologies, Ltd. include RECTOSIGHT RS300-04;AND PROTOSIGHT PS300-04 DEVICE, RECTOSIGHT RS 300-04 and COLONOSIGHT MODEL 510B.