# K173692: D-Actor 200 Vibration Massage System

- Pathway: 510(k) (Traditional)
- Applicant: Storz Medical AG
- Decided: Apr 13, 2018 after 133 days
- Product code: ISA (Massager, Therapeutic, Electric)
- Device class: 1
- Regulation: 21 CFR 890.5660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K943450 (1995). 191 ancestors in all.
6 later devices descend from it; 5 cite it directly.
0 of 198 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081541: Dermablate Effect, Asclepion Laser Technologies GmbH (2009) Summary page 4.
- K112669: Tattoostar Effect Y, Asclepion Laser Technologies GmbH (2012) Summary page 4.

## Most influential descendants
- K210451: OrthoGold 100 (2021), 2 descendants of its own
- K220538: DolorClast Radial (2022), 1 descendant of its own
- K243488: Vmat Pro (2025), 0 descendants of its own
- K221865: BTL-094 (2023), 0 descendants of its own
- K210166: Omnispec ED1000 (2023), 0 descendants of its own

## Indications for use
The D-ACTOR® 200 Vibration Massage System is intended for: • Relief of minor muscle aches and pains • Temporary increase in local blood circulation • Activation of connective tissue

Source page: https://510kreport.com/device/K173692
Methodology: https://510kreport.com/methodology