Paris Contact Lens Laboratory
Country not established
- Devices
- 1
What Paris Contact Lens Laboratory makes
Paris Contact Lens Laboratory manufactures the Keratoplasty Suturing Lens, a specialized optical device designed for corneal transplantation procedures. This lens aids in stabilizing the cornea during suturing to improve precision and reduce postoperative complications.
The Keratoplasty Suturing Lens is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Keratoplasty Suturing Lens Ref K802593
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paris Contact Lens Laboratory have in the registry?
The registry currently lists 1 device for Paris Contact Lens Laboratory. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paris Contact Lens Laboratory's devices?
Among its 1 most recently registered device, Paris Contact Lens Laboratory has devices listed in FDA 510(k) (1 device).
What are the newest devices from Paris Contact Lens Laboratory in the registry?
The most recently registered devices listed for Paris Contact Lens Laboratory include KERATOPLASTY SUTURING LENS.