Medical Device Manufacturer · US , New Port Riche , FL

Purilens, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

Total

Cleared

Denied

Purilens, Inc. has 2 FDA 510(k) cleared medical devices. Based in New Port Riche, US.

Historical record: 2 cleared submissions from 1999 to 2000. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Purilens, Inc. Filter by specialty or product code using the sidebar.

Purilens, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Purilens, Inc.

2 devices

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