B*G*MAKEOVERS ADVANCED SKIN CARE AND SPA

FDA Device Registration & Listing · Raymond, NH, US · Registration 3027725665

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3027725665
FEI Number
3027725665
Entity Name
B*G*MAKEOVERS ADVANCED SKIN CARE AND SPA
City/State/Country
Raymond, NH, US
Establishment Address
BG Makeovers Advanced Skin Care, 6 Freetown Rd 2, 6 Freetown Rd 2, Raymond, NH 03077, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
B*G*MAKEOVERS Advanced Skin Care and Spa (Owner Number: 10088521)
Owner / Operator Contact Address
BG Makeovers Advanced Skin Care, 6 Freetown Rd 2, 6 Freetown Rd 2, Raymond, NH 03077, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230100
PMA Number
N/A

All Registered Proprietary Names

Intense Pulse Light System Ultimate Skin Refiner Platinum Pro HIFU

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect General, Plastic Surgery Class 2 878.4810 2025-06-30
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2023-08-07
OHV Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption General, Plastic Surgery Class 2 878.4590 2025-11-19

Official Correspondent

Brenda Gilbert

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

B*G*MAKEOVERS Advanced Skin Care and Spa
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K192521 Shangdong Huamei Technology Co., Ltd. Intense Pulsed Light Treatment System 2019-12-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027725665. Last updated year: 2026. Please use registration number 3027725665 when referencing this establishment in official correspondence.
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