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FORUM BRANDS, LLC

US

Last updated May 27, 2026

What FORUM BRANDS, LLC makes

The company produces unscented menstrual tampons and pads, basic male condoms made from Hevea latex, and sexual lubricants. These products are designed for personal hygiene and intimate health applications, with a focus on simplicity and accessibility.

The portfolio includes devices classified as Class I and Class II under FDA regulations, all of which are listed in the FDA’s Unique Device Identifier (UDI) system. The company operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Forum Brands, LLC primarily manufacture?

Forum Brands, LLC specializes in personal hygiene and intimate health products, including unscented menstrual tampons and pads, basic male condoms made from Hevea latex, and sexual lubricants. These devices are designed for everyday use and are categorized under FDA regulations as either Class I or Class II, depending on their intended purpose and risk level.

Where is Forum Brands, LLC based, and how does that affect its regulatory standing?

Forum Brands, LLC is based in the United States, which means its devices are subject to FDA regulations. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) system, ensuring traceability and compliance with U.S. regulatory requirements. Being based in the U.S. also means its devices are designed to meet domestic regulatory standards.

Which regulatory registries or databases list Forum Brands, LLC’s devices?

Forum Brands, LLC’s devices are included in the FDA’s Unique Device Identifier (UDI) system. This database helps track and identify medical devices in the U.S. market, ensuring transparency and regulatory compliance for products like tampons, condoms, and lubricants.

How are Forum Brands, LLC’s devices classified under FDA regulations?

Forum Brands, LLC’s devices are classified as either Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential health impact.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
mylola.com
LinkedIn
—
Facebook
—
Phone
1866-232-0970
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
055659749

Catalogue (18)

DeviceModel / ReferenceRegistriesClassStatus
Lola 24CT Large (55mm) Ultra Thin Condoms
FDA UDI
Class IIActive
Lola 8CT Light Compact Applicator Tampons
FDA UDI
Class IIActive
Lola 20 count super+ compact applicator organic cotton tampons
FDA UDI
Class IIActive
Lola 8 CT SUPER NON-APPLICATOR TAMPONS
FDA UDI
Class IIActive
Lola 8CT Super Compact Applicator Tampons
FDA UDI
Class IIActive
Lola 12CT Large (55mm) Ultra Thin Condoms
FDA UDI
Class IIActive
Lola 20 count super compact applicator organic cotton tampons
FDA UDI
Class IIActive
Lola 20 count regular compact applicator organic cotton tampons
FDA UDI
Class IIActive
Lola 24ct Ultra Thin Lubricated Condoms
FDA UDI
Class IIActive
Lola 8 CT SUPER+ NON-APPLICATOR TAMPONS
FDA UDI
Class IIActive
Lola 8CT Super + Compact Applicator Tampons
FDA UDI
Class IIActive
Lola Personal Lubricant
FDA UDI
Class IIActive
Lola 36 count organic cotton ultra thin liners
FDA UDI
Class IActive
Lola 12ct Ultra Thin Lubricated Condoms - .COM
FDA UDI
Class IIActive
Lola 12 count organic cotton ultra thin pads w/wings
FDA UDI
Class IActive
Lola 8CT Regular Compact Applicator Tampons
FDA UDI
Class IIActive
Lola 20 count light compact applicator organic cotton tampons
FDA UDI
Class IIActive
Lola 28 count organic cotton ultra thin liners
FDA UDI
Class IActive

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