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Trojan G Condom

FDA UDI

Class II (US FDA UDI)

by Church & Dwight Co., Inc.

Identity

Trade Name
Trojan G Condom FDA UDI
Generic Name
Basic male condom, Hevea-latex FDA UDI
Device Name
Trojan G Condom designed to Stimulate Her with micro ribbing on top of condom. FDA UDI
Model / Reference
00022600999317 FDA UDI
Description
Trojan G Condom designed to Stimulate Her with micro ribbing on top of condom. FDA UDI

Identifiers

Primary DI / UDI-DI
00022600999317 FDA UDI
510(k) Number
K902772 FDA UDI
FDA Product Code
HIS FDA UDI
GMDN Term
Basic male condom, Hevea-latex FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic male condom, Hevea-latex

Trojan G Condom by Church & Dwight Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic male condom, Hevea-latex.

Cleared under the same submission

K902772 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 200293d8-6b4f-4620-a4de-c191f6a2922a 35 fields · synced Jun 9, 2026