FDA 510(k) Applications Submitted by Lelo Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K160644 03/07/2016 Lelo Hex Natural Rubber Latex Condom LELO Inc.
K162511 09/08/2016 LELO RESPECT HEX Natural Rubber Latex Condom LELO INC.
K243421 11/04/2024 Lelo Hex Lubricated Natural Rubber Latex Condom Lelo Inc.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact