# K153704: Strive

- Pathway: 510(k) (Abbreviated)
- Applicant: Djo, LLC
- Decided: Jun 3, 2016 after 163 days
- Product code: GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief)
- 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: 5 generations back to K881114 (1988). 27 ancestors in all.
24 later devices descend from it; 3 cite it directly.
0 of 52 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061650: Select Tens, Model 4600S, Empi (2007) Summary page 5.
- K124016: Empi Phoenix, Djo, LLC (2013) Summary page 5.
- K131159: Smartrelief, Chattem, Inc. (2013) Summary page 5.

## Most influential descendants
- K170903: Compex Wireless USA (2017), 10 descendants of its own
- K182203: JKH Stimulator Plus (2019), 7 descendants of its own
- K191151: JKH Stimulator Plus (2019), 4 descendants of its own
- K170918: Compex Sport Elite (2017), 4 descendants of its own
- K190966: Katalyst Training System (2020), 3 descendants of its own

## Indications for use
The Strive™ TENS device is used for the symptomatic relief and management of chronic, intractable pain and relief of pain associated with arthritis. It is also used as an adjunctive treatment for post-surgical and post-trauma acute pain. As a TENS device, indications are for the following conditions: - Symptomatic relief and management of chronic, intractable pain - Adjunctive treatment for post-surgical and post-trauma acute pain - Relief of pain associated with arthritis The Strive™ TENS device is used for: -temporary relief of pain associated with sore and aching muscles due to strain from exercise or normal household and work activities. -the symptomatic relief and management of chronic, intractable pain and relief of pain associated with arthritis.

Source page: https://510kreport.com/device/K153704
Methodology: https://510kreport.com/methodology