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Okamoto USA, Inc. FDA Approvals
0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.
Newest first
A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.
| Product |
|---|
| Male Latex Condom HA510(k)May 4, 2026Obstetrics/Gynecology |
| 0.04 ZERO ZERO FOUR Male Latex Condom510(k)Feb 18, 2025Obstetrics/Gynecology |
| Okamoto 002 Lubricated Polyurethane Male Condom510(k)Feb 25, 2022Obstetrics/Gynecology |