Johari Digital Healthcare , Ltd.
Johari Digital Healthcare , Ltd. has 0 FDA recalls, 4 inspections, 10 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jul 17, 2025 · VAI
- Latest 510(k)
- Apr 27, 2023
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 10 | Oct 4, 2026 | Not stated | Current |
| Inspections | 4 | Oct 23, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Jul 17, 2025 | Jodhpur, India | Devices | Voluntary Action Indicated (VAI) | 3005154439 |
| Jul 19, 2018 | Jodhpur, India | Devices | No Action Indicated (NAI) | 3005154439 |
| Jun 10, 2015 | Jodhpur, India | Devices | No Action Indicated (NAI) | 3005154439 |
| Feb 24, 2011 | Jodhpur, India | Devices | Voluntary Action Indicated (VAI) | 3005154439 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K213078 | Myolift QT | Apr 27, 2023 |
| K212866 | truSculpt flex | Dec 3, 2022 |
| K192039 | Torc Body | Mar 29, 2020 |
| K131291 | TORC BODY | Jun 14, 2013 |
| K112351 | ULTRA BEAUTY | Mar 30, 2012 |
| K102190 | WINSTIM | Mar 17, 2011 |
| K090052 | CRANIAL ELECTRICAL NERVE STIMULATOR, MODEL FM 10/C | May 29, 2009 |
| K062439 | POWERTONE, MODEL PT-11 | Jan 8, 2007 |
| K060246 | INFREX | May 5, 2006 |
| K024036 | PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000 | Dec 20, 2002 |