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Product identity
What was that, exactly?
Type the name as it was said to you or printed on the box — or a number from it: an NDC, a device identifier or full UDI, a 510(k), PMA or application number. A name is matched against this site’s registry; a number can be looked up in FDA’s own records, with any recall filed under it. A match says a record exists. It never says the vial or device in front of you is that product.
Try:
A 510(k) number. Press the lookup button to search FDA records.
Super Hair Removal (SHR) mode: temporary hair reduction
810 nm and 755 nm applicators (HR and SHR modes): permanent reduction in hair regrowth, defined as a long-term, stable reduction in hairs regrowing at 6, 9 and 12 months after treatment
Use on all skin types (Fitzpatrick I-VI), including tanned skin, in HR and SHR modes
Diode laser modules for dermatology procedures requiring coagulation; Trio module HR mode also for benign vascular and vascular-dependent lesions
Checking it’s the real thing
No FDA authenticity notice is recorded for this product. Ask: “What’s the brand name printed on the box, vial or device panel — and may I see it?”
Look it up in FDA and National Library of Medicine databases: the record it belongs to, who holds it, and any recall or enforcement report filed under it.
Sends only “K230371” to this site, which asks FDA and the National Library of Medicine. Nothing else on this page or in your Booking File is sent, and nothing is stored.
Your booking file
Record what you found
Did you see Soprano Titanium itself — the box, vial or device panel?
Your file lives in this browser. Recording waits until it has been read.