Okamoto USA, Inc.
Okamoto USA, Inc. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 2026.
Top product codes for Okamoto USA, Inc.
Recent clearances by Okamoto USA, Inc.
- K252622 — Male Latex Condom HA
- K243584 — 0.04 ZERO ZERO FOUR Male Latex Condom
- K203541 — Okamoto 002 Lubricated Polyurethane Male Condom
- K192669 — Extremely Thin 003, ZERO ZERO THREE
- K141256 — OKAMOTO STUDDED CONDOM
- K140379 — MEGA BIG BOY CONDOM
- K090259 — OKAMOTO ULTRA THIN
- K952393 — OKAMOTO CONDOM
- K902804 — EXTEND STABILITY DATE FOR CONDOM W/SPERM LUBRICANT
- K896339 — MODIFIED LABELING ON OKAMOTO HARMONY CONDOM
- K884402 — EXTRA STRENGTH SKIN LESS SKIN CONDOM
- K884401 — SKIN LESS SKIN CONDOM W/SPERMICIDAL LUBRICANT
- K875111 — RUBBER CONTRACEPTIVE, LATEX CONDOMS
- K872664 — SKINLESS SKIN-HARMONY CONDOMS
- K872812 — SKINLESS-SKIN, PINK TINT (CONDOM)
Data sourced from openFDA. This site is unofficial and independent of the FDA.