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Hydrafacial LLC

Active in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000004431 FEI 3016453096

Hydrafacial LLC is a medical device manufacturer based in the United States, with 44 devices listed in FDA GUDID and EUDAMED (FDA Class I and II; EU Class I and IIa) as of 13 Nov 2026.

Devices
44
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 35
  • EUDAMED 16

A device listed in two registries counts in both.

Device classes
  • FDA Class I 15
  • FDA Class II 13
  • EU Class I 12
  • EU Class IIa 4
Sites and related companies
Identifiers
  • EUDAMED SRN US-MF-000004431
  • FDA FEI 3016453096
  • DUNS 364134791

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI
Authorised rep.
E C Rep LimitedIE

What Hydrafacial LLC makes

Hydrafacial LLC makes dermatological laser beam guiding handpieces, skin abrasion units, cosmetic red-light phototherapy systems, skin photodynamic therapy/phototherapy lamps, and surgical plume evacuation systems. Examples of their devices include the Hydrafacial Syndeo, Del Sol Blue Light Therapy System, and SAFE System Surgical Smoke Evacuator.

The company's portfolio is regulated under Class I, Class II, and Class IIa devices and is listed in the Eudamed and FDA UDI registries. Hydrafacial LLC is based in the US.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue44

Newest first, rows 1-44 of 44

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Rows 1-44 of 44

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000004431
FDA FEI number
3016453096
DUNS number
364134791
EUDAMED status
Active
EUDAMED registered name
Hydrafacial, LLC
Registered address
3600, E. Burnett Street, 90815, Long Beach, CA, United States
Phone
+1 562 391 2047
PRRC contact
Loraine Argyle(public in EUDAMED)

Frequently asked questions

How many devices does Hydrafacial LLC have in the registry?

The registry currently lists 44 devices for Hydrafacial LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hydrafacial LLC's devices?

Among its 44 most recently registered devices, Hydrafacial LLC has devices listed in EUDAMED (16 devices) and FDA GUDID (35 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Hydrafacial LLC's devices fall under?

Among its 44 most recently registered devices, the classes recorded for Hydrafacial LLC's devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hydrafacial LLC in the registry?

The most recently registered devices listed for Hydrafacial LLC include Hydrafacial™ Syndeo™ BLACK 240V KOREA 240V Black, Non Medical, SKINSTYLUS STERILOCK MICROSYSTEM, SKINSTYLUS STERILOCK 12-PIN CARTRIDGE IN POUCH 10445 and Hydrafacial™ Elite System, 240V INTERNATIONAL 240V Black, Non Medical.

Generated automatically from registry data and not verified by a human reviewer.