FDA.reportPublic FDA data

HydraFacial LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30164530963016453096HydraFacial LLC1N2026-01-013600 E. Burnett St. Long Beach CA US 90815

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00810007531311Hydrafacial MD Elite - 220-240VAC, 50/60Hz, 8A8006034996regulatory@hydrafacial.com
00810007531540Hydrafacial MD Elite - 100–120VAC, 50/60Hz, 8A8006034996regulatory@hydrafacial.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2369671202917254K253002SkinStylus SteriLock MicroSystem (MP1209SL)QAI2026-02-19
2369671343064647K231073SkinStylus SteriLock® MicroSystem, Model Number MP1209SLQAI2023-07-28
2369671093898124K200044SkinStylus SteriLock MicroSystemQAI2020-04-10
2369671645858086K072399DEL SOL RED LIGHT THERAPY SYSTEMILY2008-05-23
2369671275830709K061470DEL SOL BLUE LIGHT THERAPY SYSTEMGEX2006-07-20
2369671139040538

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QAI32026-02-19
ILY12008-05-23
GEX12006-07-20

GUDID#