RecallHawk

TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant

Church & Dwight Co., Inc.

Summary

Church & Dwight Co., Inc. received 510(k) clearance for TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant, a HIS device. Cleared on 2022-07-14.

Details

Source

510(k) Clearance

External ID

K221431

Action Date

2022-07-14

Status

Traditional

Category

device

Product Code

HIS

Product Description

TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant. Product code: HIS.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Church & Dwight Co., Inc. has received 4 total clearances in our database.

Church & Dwight Co., Inc. has 5 FDA actions in our database, including 1 recall and 4 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Church & Dwight Co., Inc. have FDA actions?

Church & Dwight Co., Inc. has 5 FDA actions in our database, including 1 recall and 4 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K221431" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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