Male Latex Condom
FDA 510(k) K203536 · Global Protection Corp.
510(k) numberK203536
Submission
- Device name
- Male Latex Condom
- Applicant
- Global Protection Corp.
Boston, MA, US - Received
- December 3, 2020
- Decision date
- September 3, 2021
- Decision
- Substantially Equivalent (SESE)
- Type
- Abbreviated 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- HIS – Condom
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.5300
- Specialty
- Obstetrics/Gynecology
Other 510(k)s with product code HIS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252622 | Male Latex Condom HAHIS · Abbreviated | Okamoto USA, Inc. | 05/04/2026SE |
| K252521 | LifeStyles® HydraFeel Natural Rubber Latex CondomHIS · Abbreviated | Suretex Limited | 11/18/2025SE |
| K250034 | Natural rubber latex male condomHIS · Traditional | Shaoguan Regenex Pharmaceuticals Co., Ltd. | 07/11/2025SE |
| K243421 | Lelo Hex Lubricated Natural Rubber Latex CondomHIS · Traditional | Lelo, Inc. | 03/07/2025SE |
| K243640 | Trojan Ultra Ribbed Ecstasy latex condom with lubricant (Trojan Ultra Ribbed Ecstasy)HIS · Traditional | Church & Dwight Co., Inc. | 02/21/2025SE |
| K243584 | 0.04 ZERO ZERO FOUR Male Latex CondomHIS · Abbreviated | Okamoto USA, Inc. | 02/18/2025SE |
| K232279 | LifeStyles NRL Textured CondomHIS · Abbreviated | Suretex Limited | 10/05/2023SE |
| K230049 | SKORE Smooth, Dotted, Thin Condoms - SKORE Blues, SKORE Belgian Chocolate, SKORE Dots…HIS · Traditional | Ttk Healthcare Limited | 09/07/2023SE |
| K222611 | Male Latex CondomsHIS · Traditional | Suzhou Colour-Way New Material Co., Ltd. | 11/28/2022SE |
| K220489 | Durex Patronus CloseFit, Durex Patronus RegularHIS · Traditional | Rb Health (Us), LLC | 11/07/2022SE |
More from Rb Health (Us), LLC
| 510(k) | Device | Decision |
|---|---|---|
| K250142 | Water-based LubricantNUC · Traditional | 08/08/2025SE |
| K243972 | Plain Water-based LubricantNUC · Traditional | 08/08/2025SE |
| K243967 | ONE Nitrile CondomMOL · Traditional | 04/08/2025SE |
| K240896 | ONE Nitrile CondomMOL · Traditional | 08/23/2024SE |
| K223214 | Powder-Free Nitrile Examination GlovesLZA · Abbreviated | 09/21/2023SE |
| K213087 | Natural Rubber Latex Ultrasound Transducer Probe CoversITX · Traditional | 06/07/2022SE |
| K193578 | Non-spermicidal Lubricated Male Latex CondomHIS · Abbreviated | 08/20/2020SE |
| K024324 | Latex Condom and Latex Condom Lubricated with NONOXYNOL-9HIS · Abbreviated | 03/25/2003SE |
| K960552 | Knight Light Nonlubricated CondomHIS · Traditional | 11/20/1997SE |
Questions and answers
When was Male Latex Condom cleared by the FDA?
Male Latex Condom (K203536) received a 510(k) decision of Substantially Equivalent on September 3, 2021, 274 days after the submission was received.
What is the product code of K203536?
The FDA product code is HIS – Condom, a Class II (moderate risk) device regulated under 21 CFR 884.5300.