The Sanborn Co.
Country not established
- Devices
- 2
What The Sanborn Co. makes
The Sanborn Co. manufactures the SURG-K Surgical Keratometer, a device used to measure corneal curvature for preoperative planning in eye surgeries, and the VKG 1000 Video Keratograph, which captures corneal topography and tear film dynamics for ophthalmic assessments.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Surg-K Surgical Keratometer Ref K901553
Regimes: 510(k) Registry: 510(k)Vkg 1000, Video Keratograph Ref K901523
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Sanborn Co. have in the registry?
The registry currently lists 2 devices for The Sanborn Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Sanborn Co.'s devices?
Among its 2 most recently registered devices, The Sanborn Co. has devices listed in FDA 510(k) (2 devices).
What risk classes do The Sanborn Co.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Sanborn Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from The Sanborn Co. in the registry?
The most recently registered devices listed for The Sanborn Co. include SURG-K SURGICAL KERATOMETER and VKG 1000, VIDEO KERATOGRAPH.