Registry · products & devices
What’s on the menu, and what we could verify.
56 products and devices named on spa and med spa menus. Where there is an FDA pathway and record, it is here, with what it’s authorized for, what the label warns about, and how to check it’s the real thing. Where there isn’t, the entry says unverified — that is a finding, not a gap we filled in.
Checked Sep 14, 2026. Being listed here isn’t an endorsement; it means we looked.
Only have a nickname, or a word from the box? Check a name.
Neurotoxins
6- Botox CosmeticAbbVie (Allergan Aesthetics)Licensed biologic (FDA)BLA 103000
- DysportIpsen Biopharm Ltd (BLA holder); Galderma Laboratories, L.P. (named distributor on label)Licensed biologic (FDA)BLA 125274
- XeominMerz Pharmaceuticals, LLCLicensed biologic (FDA)BLA 125360
- JeuveauEvolus, Inc. (manufactured by Daewoong Pharmaceutical Co., Ltd.)Licensed biologic (FDA)BLA 761085
- DaxxifyRevance Therapeutics, Inc.Licensed biologic (FDA)BLA 761127
- LetyboHugel, Inc.Licensed biologic (FDA)BLA 761225
Hyaluronic acid fillers
21- Juvéderm Voluma XCAllergan Aesthetics (AbbVie)FDA-approved medical device (PMA)P110033
- Juvéderm Volbella XCAllergan Aesthetics (AbbVie)FDA-approved medical device (PMA)P110033/S018
- Juvéderm Vollure XCAllergan Aesthetics (AbbVie)FDA-approved medical device (PMA)P110033/S020
- Juvéderm Ultra XCAllergan Aesthetics (AbbVie)FDA-approved medical device (PMA)P050047/S044
- Juvéderm Volux XCAllergan Aesthetics (AbbVie)FDA-approved medical device (PMA)P110033/S065
- SkinVive by JuvédermAllergan Aesthetics (AbbVie)FDA-approved medical device (PMA)P110033/S059
- Restylane-LGalderma (PMA applicant: Q-Med AB)FDA-approved medical device (PMA)P040024/S039
- Restylane LyftGalderma (PMA applicant: Q-Med AB)FDA-approved medical device (PMA)P040024/S073
- Restylane SilkGalderma (PMA applicant: Q-Med AB)FDA-approved medical device (PMA)P040024/S072
- Restylane KysseGalderma (PMA applicant: Q-Med AB)FDA-approved medical device (PMA)P140029/S021
- Restylane ContourGalderma (PMA applicant: Q-Med AB)FDA-approved medical device (PMA)P140029/S032
- Restylane DefyneGalderma (PMA applicant: Q-Med AB)FDA-approved medical device (PMA)P140029
- Restylane RefyneGalderma (PMA applicant: Q-Med AB)FDA-approved medical device (PMA)P140029
- Restylane EyelightGalderma Laboratories, L.P.FDA-approved medical device (PMA)P040024/S135
- RHA 2Teoxane S.A.FDA-approved medical device (PMA)P170002
- RHA 3Teoxane S.A.FDA-approved medical device (PMA)P170002
- RHA 4Teoxane S.A.FDA-approved medical device (PMA)P170002
- RHA RedensityTeoxane S.A.FDA-approved medical device (PMA)P170002/S012
- Belotero BalanceMerz North America, Inc.FDA-approved medical device (PMA)P090016
- Belotero Balance (+)Merz North America, Inc.FDA-approved medical device (PMA)P090016/S050
- Revanesse VersaProllenium Medical Technologies, Inc.FDA-approved medical device (PMA)P160042
Biostimulators
3Fat-reduction injectables
1Hyaluronidase
2Threads
2Exosome products
1RF microneedling
4- Morpheus8InMode Ltd. (510(k) applicant: InMode MD Ltd.)FDA-cleared device (510(k)) — cleared, not approvedK192695
- Vivace RF microneedlingSung Hwan E&B Co., Ltd. / ShenB Co., Ltd. (510(k) applicants)FDA-cleared device (510(k)) — cleared, not approvedK150409
- Potenza RF microneedlingJeisys Medical Inc. (510(k) holder)FDA-cleared device (510(k)) — cleared, not approvedK192545
- Secret RFILOODA Co., Ltd. (510(k) applicant)FDA-cleared device (510(k)) — cleared, not approvedK170325
Microneedling devices
1Lasers
9- Fraxel laserSolta MedicalFDA-cleared device (510(k)) — cleared, not approvedK242142
- Clear + BrilliantSolta Medical, Inc.FDA-cleared device (510(k)) — cleared, not approvedK223647
- Halo hybrid fractional laser by ScitonSciton, Inc.FDA status not confirmed
- PicoSureCynosure, LLCFDA-cleared device (510(k)) — cleared, not approvedK210226
- PicoWayCandela CorporationFDA-cleared device (510(k)) — cleared, not approvedK220853
- GentleMax Pro PlusCandela CorporationFDA-cleared device (510(k)) — cleared, not approvedK201111
- Soprano TitaniumAlma Lasers, Inc.FDA-cleared device (510(k)) — cleared, not approvedK230371
- Splendor XBios S.R.L. (510(k) applicant)FDA-cleared device (510(k)) — cleared, not approvedK243445
- Elite iQ (Cynosure)CynosureFDA status not confirmed
Pulsed light (IPL)
1Radiofrequency devices
1Ultrasound devices
1Cryolipolysis (fat freezing)
1Electromagnetic devices
1Hydradermabrasion devices
1Worth knowing
What an FDA record can and can’t tell you
FDA records show what was authorized, for what, and when.
They can’t show that the product in the room is authentic, in date, stored properly, or being used for its authorized purpose. Those are questions for the room.