Eight databases. Eight tabs.
510(k), MAUDE, recalls, classification, GUDID — each one is a separate website. Complizen searches all of them in one go.
FDA database search
Describe your device. Complizen searches every FDA database — clearances, adverse events, recalls, guidance — and returns the records that matter, each linked to its FDA page.
The records you need are spread across eight databases that don’t share data. Pulling everything for one device can take half a day.
510(k), MAUDE, recalls, classification, GUDID — each one is a separate website. Complizen searches all of them in one go.
So much of the FDA record lives inside PDFs you can't search. You find an entry, open the file, and read the whole thing just to see if it's relevant. Complizen reads them for you.
You search, export, read PDFs, and still wonder if you missed one. Complizen returns every match, ranked, with no duplicates.
“I used to spend half a day searching FDA databases for one answer. Complizen gets me there in five minutes.”
Leah GustkeSr. RA Specialist, Exodus New Ventures
No tabs to switch, no PDFs to dig through. Describe your device and Complizen does the searching.
Type it in plain words, the way you'd explain it to a colleague. Complizen works out the device class, product code, and CFR section for you.

510(k), MAUDE, recalls, classification, guidance — all searched at the same time.

The closest matches to your device come first — adverse events, recalls, and guidance — each linked to its FDA page.

Add any record to your draft. Export a predicate comparison table. Done.

A 20-minute walkthrough of the platform — see exactly how it searches, ranks, and cites.
Get StartedThe same official FDA records — organized, searchable, and linked back to the source.
Every clearance since 1976, with predicates included.
16M+ adverse event reports, fully searchable.
Product codes, device classes, and CFR sections.
Class I–III recalls, linked to their MAUDE reports.
Current and draft guidance for your device type.
Device identifiers, packaging, and labeling.
Premarket approvals for Class III devices, with supplements.
Clearances, recalls, and reports for one device, together.
…plus more — we constantly add new databases...
Find predicates and precedents in minutes, with comparison tables ready to use.
Take on more clients without cutting corners. Every answer is cited.
Check the pathway and the competition early, before it reaches your RA team.
Tell us about your team and what you’re researching. A team member follows up within one business day — with access and a walkthrough of the platform.
“The first time I searched for De Novo precedents, Complizen found decisions I’d missed after days of manual searching. That’s when I knew it would change how I work.”
Melissa HallFounder & Principal Consultant, Statera Consulting
Same public data, a better way in. FDA.gov makes you bring the product code and search one database at a time. Complizen takes a plain-English description, searches all of them at once, and ranks what's relevant to your device — every result cited.
No. Describe the device in plain English and Complizen maps the product code, classification, and CFR section for you — then searches on them.
510(k), MAUDE, recalls, classification, FDA guidance, GUDID/UDI, and TPLC — plus consensus standards — searched together in a single pass.
Complizen searches each database in full and returns every match — ranked and deduplicated, not a sampled top-10. And every result links to its FDA page, so you can check the source yourself.
SOC 2 aligned, encrypted in transit and at rest, and your device data never trains a model.
Give us 20 minutes. We’ll show you how Complizen searches every FDA database.