EU MDR · CLASS I · SPECTACLE FRAMES, LENSES, READERS

Your name is on the frame. In EU law, that makes you the manufacturer.

Specta takes eyewear brands from “we sell frames made in China” to a defensible technical file and a completed EUDAMED registration — asking you plain questions, asking your factory in Chinese, and explaining every step before you approve it.

122 requirements · 116 verified against primary sources · every one carries its legal citation — the full registry is available to signed-in clients, reviewers and advisors.

Nothing is invented

Every sentence in your file binds to a document you uploaded or a legal clause we cite. A validator rejects anything unbound — there is no override switch.

Your factory is asked precisely

Missing evidence becomes a one-page request in Simplified Chinese naming the document, the clause and the exact standard edition. Wrong editions bounce automatically, with the reason.

You sign informed, or not at all

Each step teaches before it asks for your approval. Before the final declaration you pass a short comprehension check — because a signature you can’t explain won’t protect you.

Eight steps, one dossier

From “what even is this product, legally?” to a registered device with ongoing surveillance.

  1. M1 Scope, role and classification
  2. M2 Foundation
  3. M3 Evidence
  4. M4 Clinical evaluation
  5. M5 Product information
  6. M6 Declare
  7. M7 Register
  8. M8 Keep

You answer the business facts once. Specta determines — with citations — what your product is, which law applies and who the legal manufacturer is; collects and checks the evidence from your factory; writes the technical file under a citation validator; and prepares your EUDAMED registration package, validated against the official schemas before anything is submitted.

Three faces, one engine

For brands & chains

Plain language, your facts

One question at a time, in your words. Every explanation carries what it means for you, what happens if it is ignored, and where the law says so. No jargon on the main path — ever.

For your factories

一页一个请求 — one request per page

No accounts, no English, no guessing. A link opens exactly what is needed and why; uploads are checked on arrival, and anything wrong comes back immediately with the reason, in Chinese.

For the record

Built to be audited

An append-only, hash-chained log of every approval, every rejection and every generated sentence — exportable and verifiable by a third party without trusting us.

The clock is real. Devices already on the market must be registered in EUDAMED by 27 November 2026 — within 12 months of the functionality notice published on 27 November 2025. Continued supply after that date is unlawful, per device, per shipment, per day.