FDA 510(k) Applications Submitted by OKAMOTO U.S.A., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090259 | 02/02/2009 | OKAMOTO ULTRA THIN | OKAMOTO U.S.A., INC. |
| K140379 | 02/14/2014 | MEGA BIG BOY CONDOM | OKAMOTO U.S.A., INC. |
| K141256 | 05/14/2014 | OKAMOTO STUDDED CONDOM | OKAMOTO U.S.A., INC. |
| K192669 | 09/25/2019 | Extremely Thin 003, ZERO ZERO THREE | Okamoto U.S.A., Inc. |
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