Frequently Asked Questions (FAQ)

DermaClip is an Rx-only medical device. To place an order, complete the Rx Authorization form on our website and a member of the team will confirm your eligibility before your first order is processed.

For a non-prescription option, DermaQuik is the over-the-counter version of DermaClip, available to anyone at DermaQuik.com. It's ideal for first aid kits and can be used by anyone, anytime skin needs to be closed.

DermaClip does not contain natural rubber latex.

DermaClip uses a top-of-the-line, long-duration, pressure-sensitive alkylate-based adhesive - adhesive enhancers are not required for typical use. That said, enhancers can be used if preferred or if your protocol calls for them. If using enhancers on patients with fragile or aging skin, exercise caution: enhancers may increase adhesion beyond what fragile skin can tolerate and could cause damage upon removal.

Yes. Visit our Request Evaluation Samples page or email us at samples@dermaclip.com with your facility information and NPI number and a member of the team will follow up.

DermaClip US, LLC primarily ships within the United States. We do ship internationally, but only to licensed medical device distributors in the destination country. We currently have distribution arrangements in Panama and Costa Rica. For international inquiries, contact us at info@dermaclip.com.

DermaClip is classified as a "Tape and Bandage, Adhesive" under FDA product code KGX - a Class I, 510(k) exempt device. DermaClip has confirmed its classification with the FDA and is a registered device.

DermaClip has three main components, all manufactured and purchased in the United States. The device uses two FDA-registered medical grade adhesives and a food-grade plastic sourced from a US-based petrochemical facility. Final assembly takes place in Mexico.

All manufacturing facilities are FDA registered and comply with Good Manufacturing Practices (GMP) as required under the FDA's Quality Systems Regulation (QSR).

Manufacturing facilities are FDA registered and subject to FDA QSR requirements. In addition, manufacturing operations are certified to ISO 13485, the international standard for medical device quality management systems.

DermaClip utilizes ETO (ethylene oxide) sterilization.

DermaClip is available through the Premier GPO.

DermaClip is carried by McKesson, Henry Schein, Owens & Minor, and Performance Health (MedCo). For distributor item numbers and ordering information, visit our Ordering page.