About Us

We built Snorbliss® because a friend couldn’t sleep.

Snorbliss began in January 2025 with a problem that was personal to us. One of our closest friends had been struggling with persistent snoring, and together we tried nearly every solution — even the possibility of CPAP. Some options offered only temporary relief; others felt too complicated, too bulky or too uncomfortable to use night after night. When we found mandibular advancement mouthpieces, the principle made sense but the experience did not. So rather than accept that discomfort was unavoidable, we decided to build a better one.

3 U.S. CLINICS

6 PROTOTYPE GENERATIONS

120 ADULT WEARERS

FDA CLEARED · K261251

ENDEAVOR COMMERCE, LLC

MEET SNORBLISS PRO 2.0

Snorbliss Pro 2.0 anti-snoring mouthpiece with retail box, blue storage case and instruction manual

Six prototypes. 120 sleepers. One design we’d put our name on.

That decision led to a demanding development process built around research, professional input and repeated refinement. We collaborated with clinicians and dental technicians across three U.S. clinics, created custom molds, evaluated different tray shapes and connector positions, and rebuilt the product whenever a design failed to meet our expectations.

In total we developed six distinct prototype generations and evaluated them with 120 adult wearers, gathering structured feedback on molding, fit, stability, bulk, jaw positioning and overnight comfort.

We were never interested in releasing the first version that simply worked. We kept refining until we reached the strongest balance between adjustability, stability, lower-profile comfort and practical daily use. The final Snorbliss® Pro 2.0 combines heat-moldable fitting surfaces with a supportive rigid structure and interchangeable adjustment straps, so users can gradually personalise how far the lower jaw is advanced.

2025

Where It Started

January — one friend who couldn’t sleep

6

Prototype Generations

rebuilt until it felt right

120

Adult Wearers Tested

structured feedback on fit and comfort

3

U.S. Clinics

clinicians and dental technicians

Completing the design was only the beginning

Bringing Snorbliss® to market required a second round of investment entirely: independent laboratory testing, material evaluation, durability verification, cleaning validation, biocompatibility assessment, oral-contact testing, formal risk management and regulatory review.

On 11 June 2026 the U.S. Food and Drug Administration granted Snorbliss® its own 510(k) clearance, K261251 — a Class II, over-the-counter intraoral device for snoring under 21 CFR 872.5570. The clearance is held in our own name, Endeavor Commerce, LLC, not licensed from someone else’s file. It is a public record, and you are welcome to look it up.

Every failed mold, every uncomfortable prototype, every technical revision and every test result helped shape the product we sell today. Snorbliss® Pro 2.0 was not created from a single idea or a quick design process; it was built through persistence, collaboration, and a refusal to settle for “good enough.”

FDA 510(k) K261251 — Class II, over the counter, cleared 11 June 2026

ISO 10993-5 cytotoxicity — no cytotoxic potential

ISO 10993-23 oral mucosa irritation — no irritation effect

ISO 10993-10 sensitization — no sensitization reaction

9,125 simulated bite cycles at 10 N — no damage

Ultrasonic cleaning validated — no stains after 10 minutes

Re-molding verified across 3 heat cycles

Developed under a full ISO 14971 risk management process

SEE HOW IT WORKS

Say Only What We Can Prove

We say FDA-cleared, never “FDA-approved” — they are different pathways and only one is ours. We do not claim to treat sleep apnea, because our clearance covers snoring reduction. We cite a real 510(k) number you can look up. When the honest claim is smaller than the marketing claim, we use the honest one.

Comfort Is the Whole Product

A device you abandon in a drawer helps nobody. That is why we chased 50% less bulk, soft bite trays in a rigid frame, an oral breathing channel and four gradual settings instead of one aggressive default. The best anti-snoring device is the one you can actually sleep in.

Tell People the Hard Parts

The first 3 to 5 days can mean a sore jaw and extra saliva. You cannot talk or drink with it in. It is not for anyone under 18, anyone with TMJ problems, or anyone wearing braces at night. We publish all of it, because a customer who knows what to expect is a customer who sticks with it.

Our Own FDA Clearance

510(k) K261251, held by Endeavor Commerce, LLC

Independently Lab-Tested

ISO 10993 biocompatibility · ISO 14971 risk file

60-Night Guarantee

Sleep on it, or send it back

Real People On Support

snorbliss01@gmail.com · text +1 732 812 5665

Who makes Snorbliss®?

Snorbliss® is designed and sold by Endeavor Commerce, LLC, a U.S. company based at 30 N Gould St Ste 47051, Sheridan, Wyoming 82801. The FDA 510(k) clearance for the device, K261251, is held in our own name — we did not license it from another manufacturer’s file. The device itself is manufactured overseas with medical-grade materials.

Is Snorbliss® FDA-approved?

It is FDA-cleared, which is a different thing, and we are careful about the distinction. Snorbliss® holds 510(k) clearance number K261251, granted on 11 June 2026, as a Class II over-the-counter intraoral device for snoring under 21 CFR 872.5570, product code LRK. “FDA-approved” describes a different regulatory pathway that does not apply to this device, so you will never see us use it.

What was the product actually tested for?

The finished device passed independent ISO 10993 biocompatibility testing: ISO 10993-5 (no cytotoxic potential), ISO 10993-23 (no irritation of oral mucosa tissue) and ISO 10993-10 (no sensitization reaction), each run with both polar and non-polar extracts. Independent durability testing put it through 9,125 simulated bite cycles at 10 N with no damage, and validated ultrasonic cleaning — ten minutes left no stains. Re-molding was verified across three heat cycles. The whole device was developed under an ISO 14971:2019 risk management process, and all residual risks were evaluated as acceptable.

Do you sell anything besides the mouthpiece?

Snorbliss® is our only device. Alongside it we sell the two care products that were validated with it — an ultrasonic cleaner and a retainer cleaner foam — plus drug-free nasal strips for the nights when congestion is the problem. Because the device should be replaced every six months, we can also set you up on a replacement cycle.

What is your return policy?

Sixty nights. Mold it, work up through the straps, sleep on it. If your nights aren’t quieter, email snorbliss01@gmail.com and we refund you — no forms to fight through and no restocking fee.

How do I reach a human?

Email snorbliss01@gmail.com or text +1 732 812 5665. We read our own customer messages, and if something is wrong with your device — a crack, a loose strap, a fit you cannot get right — tell us and we will sort out a replacement.

Still have a question? Ask us directly.

Dream Deeper. Sleep Sweeter.

That has been the purpose from the very beginning: a thoughtfully developed, customizable anti-snoring device that supports quieter nights with comfort at the centre of the experience — so more people wake up to better mornings, together. Snorbliss® is intended to aid in the reduction of snoring. It is not intended to diagnose, treat, cure, or prevent sleep apnea or any disease. If you experience loud snoring with gasping or choking, excessive daytime sleepiness, or other warning signs, consult a healthcare professional.

SHOP SNORBLISS

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