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FDA Recall & Compliance Alerts for Medspa Owners
Devices & TechKorean toxin makers split as Daewoong and Hugel advancetodaySearch DemandWho Can Inject Botox and Filler in Florida: Scope of Practice and Licensure Requirements6 weeks agoBusiness & M&AHugel chases 1 trillion won in three yearsyesterdayBusiness & M&AAbbVie Files Material Event: Botox/Juvéderm Pricing Shift5 weeks agoBusiness & M&AAbbVie takes $216M charge on Q3 deals, cuts earnings3 days agoDevices & TechHebei Zollvan Diode Laser Clears FDA 510(k)4 weeks agoDevices & TechDEKA and GeoMedics expand laser portfolio across India4 days agoDevices & TechVIOL Scarlet Pro Wins FDA 510(k) Clearance4 weeks agoDevices & TechBTL expands EXOMIND brain stimulation to OCD, adolescentslast weekDevices & TechECHOLASER X4 Clears FDA 510(k) for General Surgery3 weeks agoDevices & TechSkinHealth Systems launches SkinStylus in six European marketslast weekRegulatoryAllergan gets Health Canada nod for Boey, a fast-acting short-duration toxinlast week

Inside MedSpa — Never miss a recall or a rule change.

Today's Medspa Watch — Oct 9, 2026

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Every week the FDA clears a device, a state board rewrites who can inject what, a manufacturer quietly changes its pricing. None of it is secret — the clearances, the enforcement actions, the rule changes are all published, all public, and buried in databases no practice owner has time to check. Device reps and consultants have staff for that. Now you have us.

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