Okamoto USA, Inc.
FDA 510(k) medical device clearances.
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.