Beaver-Visitec International, Inc. - FDA 510(k) Cleared Devices

Beaver-Visitec International, Inc. is a medical device company with a manufacturing facility in Waltham, US. The company specializes in Ophthalmic devices and systems for surgical and clinical applications.

The company has received 1 FDA 510(k) clearance from 1 total submission. Beaver-Visitec International, Inc. maintains a focused portfolio in the Ophthalmic category, which represents 100% of its regulatory submissions. The company achieved its first clearance in 2025 and remains active in FDA regulatory pathways.

Recent cleared devices include laser and endoscopy systems designed for ophthalmic surgical use. These products reflect the company's commitment to precision instrumentation in eye care and surgical visualization.

Explore the company's complete regulatory record, including device names, product codes, and clearance dates in the database.