For nearly 30 years, Wet® has made high-quality, innovative and unique products that are formulated using only the finest ingredients.
Founded in 1989 by Michael Trigg, Trigg Laboratories manufactures premium sexual wellness and consumer healthcare products, and is the parent company of Wet® International, Inc., one of the world’s best-selling lines of personal lubricants and intimacy products.
We develop, formulate and package Wet® products at Trigg Laboratories’ 70,000 square-foot, state-of-the-art manufacturing and distribution facility in Las Vegas, Nevada. All Wet® formulas are manufactured and tested in compliance with FDA’s strict Medical Device Quality System Regulations (QSR) and current Good Manufacturing Practices (cGMP). This ensures exceptional integrity and consistency and provides maximum comfort levels. Our new Las Vegas location will also serve as the home of our sales, marketing and administrative offices, as well as our warehousing and shipping center.
All Wet® products are created to meet the highest industry standards. From our best-selling Wet® Platinum® and Wet® Water Based® to our Strawberry Flavored®, Wet® Organics™, and our Wet® Elite Femme ® – we truly make a formula for every desire. The Wet® Brand is available in all major drugstores and mass market retailers in the U.S. and Canada, as well as more than 60 countries around the world and online stores.
Trigg Laboratories continues to grow, innovate and more importantly listens to our customers. We HEAR what you are saying and your input drives us to strive harder in developing new and unique products that deliver the high quality personal products that you have come to expect.
We believe that companies are like individuals, each creating their own “Karma.” Giving back has been paramount to us since our inception. Through our charitable giving program, we contribute to the good work of more than 300 non-profit community and educational organizations worldwide.
Trigg Laboratories has years of experience in the evolving personal lubricant market and a commitment to strict manufacturing compliance. This ensures products are manufactured on time and adhere with FDA’s Quality System Regulations (QSR), current Good Manufacturing Practices (cGMP) and ISO 13485:2016, ENISO 13485:2016 and MDSAP. Our products are FDA 510(k)’s cleared to market.
- Certified to ISO 13485:2016, ENISO 13485:2016 and MDSAP
- EU MDD, eMDR compliance
- Registered with the FDA as medical device manufacturer and Over-the-Counter (OTC) establishment licenses
- FDA Compliant manufacturing (QSR and cGMP)
- FDA 510(k) Cleared product
- Accredited UL RCP Certificate
- UL cGMP Certified
- CE mark product