Regulatory Compliance

Last Updated: September 4, 2026

Juni is a product of GlowMax, Inc. This page collects regulatory and product-compliance statements for the Juni Device. It is a template ready for certification data; bracketed items are pending.

1. United States — FCC

[PENDING CERTIFICATION] Model Number: [PENDING CERTIFICATION] — FCC ID: [PENDING CERTIFICATION]

Template statement (to be finalized upon grant of equipment authorization):

> This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. > > This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses, and can radiate radio-frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. > > Changes or modifications not expressly approved by GlowMax, Inc. could void the user's authority to operate the equipment.

The Juni Device will not be marketed or sold in the United States until required FCC equipment authorization (and any applicable RF-exposure evaluation) is complete.

2. European Union — CE

For Devices placed on the EU market, GlowMax, Inc. commits to conformity with applicable EU legislation, including the Radio Equipment Directive 2014/53/EU, EMC Directive 2014/30/EU, LVD 2014/35/EU (as applicable), and RoHS Directive 2011/65/EU. The EU Declaration of Conformity will be published at juni.skin/legal/compliance upon certification. [PENDING CERTIFICATION] — Notified Body / certificate numbers to be inserted.

3. United Kingdom — UKCA

For Devices placed on the UK market, GlowMax, Inc. commits to conformity with applicable UK regulations (Radio Equipment Regulations 2017, EMC Regulations 2016, Electrical Equipment (Safety) Regulations 2016, RoHS Regulations 2012) and to affixing UKCA marking once assessment is complete. [PENDING CERTIFICATION]

4. Disposal — WEEE

The crossed-out wheelie-bin symbol means the Device and its batteries must not be disposed of with household waste. In the EU/UK, take end-of-life Devices to a designated WEEE collection point; we will operate a take-back program at launch (legal@juni.skin) — [PENDING]. Proper disposal protects the environment and human health and enables material recovery.

4A. Medical-Device Status (EU MDR / UK MDR)

The Juni Device is assessed as a non-medical general wellness device consistent with MDCG guidance on qualification of software and wellness products; it is not placed on the market with a medical intended purpose. EU MDR 2017/745 / UK MDR pathway status: under evaluation — [PENDING]. This page will be updated if the assessment changes.

5. Responsible Person / Contact

GlowMax, Inc. dba Juni — 1111b South Governors Av #42569, Dover, DE 19904, USA — legal@juni.skin EU Authorized Representative: [PENDING — to be appointed before EU launch] UK Responsible Person: [PENDING — to be appointed before UK launch]