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NuFACE TRINITY+ Starter Kit

NuFACE TRINITY+ Starter Kit product photo

Product image: NuFACE product page.

The NuFACE TRINITY+ is a handheld microcurrent device: two rounded probes send a low-level electrical current across the skin while you glide them over your face and neck.

NuFACE describes three customizable intensities and a Boost button that raises output by 25%. Optional attachments include an Effective Lip & Eye head and a Wrinkle Reducer. The brand suggests at least 5 minutes a day, 5 days a week for 60 days, then 2–3 times a week. The FDA record shows a 510(k) clearance (K201782).

It's NuFACE's most versatile device. It's at the higher end on price for microcurrent, and it needs a conductive gel every session.

Lowest price we saw (price checked Nov 1, 2026)$395
FDA-cleared
Store-listed deal we verified: TRINITY+ 'Lift + Brighten' holiday kit: $299 (store-listed comparison price $432). Kit with TRINITY+, Aqua Gel and Silk Crème activators, brush and masks; brand shows compare-at $432. Price checked Nov 1, 2026. This is the store's own comparison, not a price history we tracked. View on store site

Prices

StorePricePrice checked / source
NuFACE (brand site)$395 Nov 1, 2026
brand store data		 View
Ulta$395 Nov 1, 2026
retailer page		 View
Sephora$395 Nov 1, 2026
retailer catalog		 View
Dermstore
15% off your first Dermstore order with code KRISTIN-R59U · Get the code (new customers only; GlowSpec's founder earns store credit. Disclosure)
$395 Nov 1, 2026
retailer catalog		 View

Store links go straight to the store's product page, with no affiliate tracking. Confirm the price there before you buy. The Dermstore code above is our referral code: our founder earns Dermstore store credit when a new customer uses it. See our disclosure.

Price history

$218 at CurrentBody (with code), 2023-07. Reported in a July 2023 sale article; not a current price. Source

Specs & regulatory status

FDA statusFDA-cleared 510(k) K201782
510(k) 'NuFace Trinity Plus Device', decided 2021-01-22.
FDA record or source

"FDA-cleared" means we matched this product to a 510(k) record: the FDA cleared it as substantially equivalent to an existing device for its labelled use. FDA clearance is not FDA approval, and a listed specification isn't proof that a device works. How we check FDA status.

Terms on this page

510(k)
The FDA premarket notification route. A cleared 510(k) means the FDA found the device substantially equivalent to one already on the market. It is not FDA approval.
Microcurrent
A low-level electrical current passed across the skin by a handheld device.