# K103031: BMR Face

- Pathway: 510(k) (Traditional)
- Applicant: Bio-Medical Research, Ltd.
- Decided: Nov 10, 2011 after 394 days
- Product code: NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K011935 (2001). 1 ancestor in all.
5 later devices descend from it; 3 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011935: Rejuvenique Model #RJV10, Salton, Inc. (2001) Summary page 4.

## Most influential descendants
- K250227: JOVS Electric Stimulation Beauty Device (JE2) (2025), 1 descendant of its own
- K244004: Microcurrent Facial Device (CEC101, EE0101, EEI101) (2025), 1 descendant of its own
- K253932: FACEGYM Pro Device (HD-109) (2026), 0 descendants of its own
- K252553: Facial & Body Beauty Device (INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507) (2025), 0 descendants of its own
- K192077: Tua Face Fitness / Tua Trend Face (2020), 0 descendants of its own

## Indications for use
BMR Face is intended for facial stimulation and is indicated for over the counter cosmetic use

Source page: https://510kreport.com/device/K103031
Methodology: https://510kreport.com/methodology