FDA 510(k) Applications Submitted by BIOTEX, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K092197 |
07/21/2009 |
PHOTEX30 DIODE LASER SERIES: 980, 810, 940 |
BIOTEX, INC. |
| K053087 |
11/02/2005 |
VISUALASE COOLED LASER APPLICATOR SYSTEM, LASER DIFFUSING FIBER, COOLING CATHETER SYSTEM |
BIOTEX, INC. |
| K063505 |
11/20/2006 |
VISUALASE ENVISION SOFTWARE SYSTEM |
BIOTEX, INC. |
| K060304 |
02/06/2006 |
PHOTEX DIODE LASER SERIES, MODELS 980, 810 AND 940 |
BIOTEX, INC. |
| K071328 |
05/11/2007 |
VISUALASE THERMAL THERAPY SYSTEM |
BIOTEX, INC. |
| K161704 |
06/20/2016 |
Phasor Drill |
BIOTEX, INC. |
| K081656 |
06/12/2008 |
VISUALASE THERMAL THERAPY SYSTEM |
BIOTEX, INC. |
| K203712 |
12/21/2020 |
The Slide |
Biotex, Inc. |
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