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Plan and retrieve
The agent builds country-specific search terms and retrieves comparable products from each selected registration database.
Free · No signup · Real registration data
South Korea Medical Device Registration Cost & Timeline Planner
Describe a product to estimate its MFDS pathway, government registration fee, dossier preparation time, review timeline, and likely registration steps.
27 supported marketsUp to 5 countries per runOfficial sources and registry records
Search similar registered products
Use actual country registration records to ground the product and pathway research.
Estimate government fees
Map the likely class to current country fee schedules and relevant fee line items.
Separate prep from review time
See dossier preparation, official review, and realistic end-to-end planning ranges.
Build a multi-market registration estimate
Include intended use, users, patient population, operating principle, contact duration, and whether the device is sterile, measuring, active, implantable, software, or an IVD.
How this free agent works
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Check and map
It checks current official sources, suggests the likely class and pathway, and maps them to maintained fee and timeline data.
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Build an actionable plan
The result separates dossier preparation from review time and lays out the likely sequence, assumptions, and missing facts.
Frequently asked questions
Open the Similar Product Finder →What costs are included in the registration estimate?
The estimate uses the current government fee schedule stored for each market. It does not include testing, audits, translations, local representation, consulting, notified-body or conformity-assessment fees unless they appear explicitly in the government schedule.
How are preparation and review time different?
Preparation time estimates the manufacturer and regulatory team’s work to create a review-ready dossier. Review time is the published or statutory regulator benchmark. The realistic end-to-end range accounts for common preparation and review delays.
Does the planner classify my device?
It suggests a preliminary class and pathway using the country scheme, current official sources, and similar registration records. The final classification depends on the complete intended use, design, labeling, and applicable current rules.
Can I compare several countries at once?
Yes. A free run can research up to five markets. Each selected country uses its own classification scheme, registration database, fee table, timeline data, and official sources.
Keep researching this market