Product code ILX— Physical Medicine
ACTIBAND
- Classification name
- Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
- Device class
- Class 2
- Regulation
- 21 CFR 890.5290
- Advisory panel
- Physical Medicine
- Total cleared
- 15
- First cleared
- Most recent
Market context for product code ILX
FDA has cleared devices under product code ILX between 1989 and 2024, filed by 11 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2024
- 2020
- 2019
- 2013
- 2012
- 2010
- 2009
- 2008
- 2007
- 2002
- 1997
- 1991
- 1989
Top applicants under product code ILX
Recent clearances under product code ILX
- K241395 — Active System; Avenue8
- K202337 — Pulsed electromagnetic field wrap
- K190251 — RecoveryRx
- K131979 — PROVANT THERAPY SYSTEM
- K121702 — ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE
- K121338 — ZEOBI
- K091791 — PROVANT SYSTEM, MODEL 4201
- K092044 — ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE
- K091996 — ORTHOCOR KNEE SYSTEM BASIC
- K070541 — IVIVI SOFPULSE, MODELS 912-M10, ROMA3 AND TORINO II
- K070931 — MODEL PMT850
- K022404 — ACTIBAND
- K972093 — REGENESIS MODEL 42
- K903675 — MAGNETIC RESONANCE THERAPY DEVICE
- K882816 — PULSAR EM
Data sourced from openFDA. This site is unofficial and independent of the FDA.