Data / Medical devices / United States / Church & Dwight Manufacturing Co., Inc.
Church & Dwight Manufacturing Co., Inc.: FDA-registered device maker in South Chesterfield, VA, United States, 21 510(k) clearances
Church & Dwight Manufacturing Co., Inc. is registered with the FDA (registration 1122329) in South Chesterfield, VA, United States. It lists 3 device types. The FDA files 21 510(k) clearances under its listings, the newest dated May 4, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1122329
- Address
- 1851 Touchstone RD, South Chesterfield, VA, United States, 23834
- Owner or operator
- CHURCH & DWIGHT CO., INC. (2210299)
- Roles
- Manufacturer, Manufacturer for export, Repackager or relabeler
- First device listed
- November 26, 2008
- Registered through
- 2027
- Brand names listed
- TROJAN HER PLEASURE (Ribbed) ECSTASY, TROJAN NaturaLamb Luxury Condom, Trojan BareSkin Raw, Trojan Charged Condom, Trojan Double Ecstasy Condom, Trojan ENZ Armor, Trojan ENZ Armor Condom, Trojan ENZ Latex Non-Lubricated Condoms and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Condom | HIS | 2 | Manufacturer, Manufacturer for export, Repackager or relabeler | accessdata.fda.gov |
| Condom With Nonoxynol-9 | LTZ | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Condom, Synthetic | MOL | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 4, 2026 | K252622 | Male Latex Condom HA | HIS | Substantially Equivalent | Okamoto USA, Inc. | accessdata.fda.gov |
| February 25, 2022 | K203541 | Okamoto 002 Lubricated Polyurethane Male Condom | MOL | Substantially Equivalent | Okamoto USA, Inc. | accessdata.fda.gov |
| July 24, 2020 | K192669 | Extremely Thin 003, ZERO ZERO THREE | HIS | Substantially Equivalent | Okamoto USA, Inc. | accessdata.fda.gov |
| August 1, 2017 | K171639 | Trojan Supra Lubricated Polyurethane Male Condom | MOL | Substantially Equivalent | Church & Dwight Co., Inc. | accessdata.fda.gov |
| July 23, 2014 | K141256 | OKAMOTO STUDDED CONDOM | HIS | Substantially Equivalent | Okamoto USA, Inc. | accessdata.fda.gov |
| July 1, 2014 | K140379 | MEGA BIG BOY CONDOM | HIS | Substantially Equivalent | Okamoto USA, Inc. | accessdata.fda.gov |
| June 19, 2012 | K120286 | TROJAN HER PLEASURE (RIBBED) ECSTASY LATEX CONDOM WITH LUBRICANT | HIS | Substantially Equivalent | Church & Dwight Co., Inc. | accessdata.fda.gov |
| May 16, 2012 | K120287 | TROJAN MAGNUM CONDOM WITH FIRE & ICE LUBRICANT | HIS | Substantially Equivalent | Church & Dwight Co., Inc. | accessdata.fda.gov |
| May 11, 2012 | K120249 | TROJAN MAGNUM CONDOM WITH WARMING LUBRICANT | HIS | Substantially Equivalent | Church & Dwight Virginia Co., Inc. | accessdata.fda.gov |
| March 31, 2009 | K090259 | OKAMOTO ULTRA THIN | HIS | Substantially Equivalent | Okamoto USA, Inc. | accessdata.fda.gov |
| October 26, 2007 | K071313 | TROJAN-ENZ BRAND | HIS | Substantially Equivalent | Church & Dwight Co., Inc. | accessdata.fda.gov |
| May 9, 2000 | K001212 | TROJAN EXTRA LARGE LATEX CONDOM | HIS | Substantially Equivalent | Armkel, LLC | accessdata.fda.gov |
| April 6, 2000 | K000748 | TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT | HIS | Substantially Equivalent | Armkel, LLC | accessdata.fda.gov |
| February 3, 1992 | K912901 | TROJAN (TM-TBD) CONDOM | HIS | Substantially Equivalent | Carter Products | accessdata.fda.gov |
| June 19, 1990 | K901202 | TROJAN NATURALAMB LUBRICATED NATURAL MODIFIED | HIS | Substantially Equivalent | Carter Products | accessdata.fda.gov |
| April 16, 1990 | K901199 | TROJAN-ENZ LATEX CONDOMS W/SPERMICIDAL MODIFIED | HIS | Substantially Equivalent | Carter Products | accessdata.fda.gov |
| April 16, 1990 | K901194 | TROJAN RIBBED LUBRI. LATEX CONDOMS MODIFIED LABEL | HIS | Substantially Equivalent | Carter Products | accessdata.fda.gov |
| April 16, 1990 | K901192 | TROJAN-ENZ LUBRI. CONDOMS (MODIFIED LABELING) | HIS | Substantially Equivalent | Carter Products | accessdata.fda.gov |
| April 16, 1990 | K901191 | TROJAN-ENZ LATEX CONDOMS (MODIFIED LABELING) | HIS | Substantially Equivalent | Carter Products | accessdata.fda.gov |
| January 23, 1990 | K895640 | MAGNUM PLUS LATEX CONDOM W/SPERMICIDAL LUBRICANT | HIS | Substantially Equivalent | Armkel, LLC | accessdata.fda.gov |
| March 7, 1988 | K874383 | MENTOR PLUS (CONDOM) | HIS | Substantially Equivalent | Arcon Corp. | accessdata.fda.gov |
Compare with other makers
Updated May 4, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.