Reach every procedural clinician where they research.

The catalog clinicians come to when they research the devices they use every day — side-by-side specs, education from the source, and reviews from world experts.

Three ways to show up

Pick the depth of presence that fits.

Every device in the GI catalog starts as a Listed page built from public FDA data. Manufacturers who want more control of their story can upgrade.

Listed

Public, auto-generated

The default for every device with an FDA 510(k) clearance.

Generated from openFDA + 510(k) data
Appears in browse + compare flows
510(k) clearance status shown
Marked as an unclaimed listing
No manufacturer involvement required

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Verified

Most claim this

Claimed + curated

Manufacturers who want to own the narrative on their products.

Everything in Listed
Verified-manufacturer badge on every page
Curated specs, descriptions, brand line
IFU + brochure PDFs hosted on the page
Photos and product imagery
Reply to clinician reviews

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Channel

Education + lead-gen

Manufacturers running active education + market-development programs.

Everything in Verified
Procedure videos + technique guides
Featured placement in subcategories
Inquiry routing from interested clinicians
Engagement analytics dashboard
Multiple team members

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Pricing is a conversation we have on a call — every manufacturer's scope and product line is different.

Built especially for

Sub-scale manufacturers and challengers

Make a great device without the Big-3's marketing budget? onescratch gives you the same reach — same clinician audience, same credibility tools: verified reviews, FDA clearance status, side-by-side comparison.

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