FDA Product Code
FDA Product Code ILX — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Physical Medicine
- 21 CFR Citation
- 890.5290
510(k) Clearances — 15 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K241395 | Active System; Avenue8 | Caerus Corporation | 2024-12-18 | Traditional | PDF ↗ |
| K202337 | Pulsed electromagnetic field wrap | Hi-Dow International, Inc. | 2020-12-15 | Traditional | PDF ↗ |
| K190251 | RecoveryRx | Bioelectronics Corporation | 2019-06-28 | Traditional | PDF ↗ |
| K131979 | PROVANT THERAPY SYSTEM | Regenesis Biomedical, Inc. | 2013-12-13 | Traditional | PDF ↗ |
| K121702 | ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE | Orthocor Medical | 2013-05-06 | Traditional | PDF ↗ |
| K121338 | ZEOBI | Ivivi Health Science, LLC | 2012-07-27 | Special | PDF ↗ |
| K091791 | PROVANT SYSTEM, MODEL 4201 | Regenesis Biomedical, Inc. | 2010-04-07 | Traditional | PDF ↗ |
| K092044 | ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE | Orthocor Medical | 2009-12-18 | Traditional | PDF ↗ |
| K091996 | ORTHOCOR KNEE SYSTEM BASIC | Orthocor Medical | 2009-12-15 | Traditional | PDF ↗ |
| K070541 | IVIVI SOFPULSE, MODELS 912-M10, ROMA3 AND TORINO II | Ivivi Technologies, Inc. | 2008-12-11 | Traditional | PDF ↗ |
| K070931 | MODEL PMT850 | Promedtek, Inc. | 2007-05-24 | Traditional | PDF ↗ |
| K022404 | ACTIBAND | Paw, LLC | 2002-08-08 | Traditional | PDF ↗ |
| K972093 | REGENESIS MODEL 42 | Regenesis Biomedical, Inc. | 1997-10-21 | Traditional | PDF ↗ |
| K903675 | MAGNETIC RESONANCE THERAPY DEVICE | Mrt, Inc. | 1991-01-17 | Traditional | PDF ↗ |
| K882816 | PULSAR EM | Apex Medical, Inc. | 1989-04-27 | Traditional | PDF ↗ |
Product code ILX · Class II · Physical Medicine. Data: openFDA.