The right FIT for BPH
™
The ProVee stent uses 3-D geometry which mirrors and engages with the anatomy of the prostate. The system alleviates Lower Urinary Tract Symptoms (LUTS) by opening the prostatic urethra, applying radial force to the prostatic lobes.
®
Enlarged prostate
An enlarged prostate can narrow or even block the urethra causing bothersome urinary symptoms
Step 1
The ProVee flexible delivery system is placed through the obstructed urethra to access the enlarged prostate
The ProVee stent is deployed, providing fast and effective relief by gently opening the obstructed urethra
Step 2
The ProVee Difference
®
Gentle
ProVee de-obstructs
with no cutting, piercing
or heating of the
prostate tissue
Rapid Recovery
Atraumatic procedure
with minimal bleeding decreasing likelihood of post-op catheterization
Precise Delivery
Controlled, targeted, accurate deployment under direct visualization
Reversible
The ProVee stent
can be easily retrieved
for any reason at
any time
Atraumatic
Low profile (16F) delivery system has the same profile as a flexible diagnostic cystoscope
Universal Fit
The ProVee novel
design provides a single
size to treat all
indicated anatomy
The ProVee Stent
®
Universal fit: The nitinol stent with an atraumatic profile is universally sized to treat all indicated anatomy
​​​No crossing struts to minimize potential encrustation
Designed to support the three dominant lobes of the prostate
Designed to accommodate the verumontanum and fit between the bladder neck and external sphincter
​​​Radial force tuned to gently push against prostatic tissue
​​Reversible: The ProVee stent can be easily retrieved for any reason at any time
The ProVee Delivery Device
®
Video processing unit (VPU) cable and connector
Steering lever
Step 2
release button
Deployment trigger
Luer connector
Preloaded ProVee stent
16F flexible sheath:
The same low proile design as a diagnostic cystoscope
The ProVee VPU
®
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Small footprint - Easily portable
​
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Attached kickstand - No IV pole or cart needed
​
-
Crisp and clear video quality
​
-
Usable at any site of service
​
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Ready to go - Simply connect with external cable from delivery device
Growing Collection of Clinical Data
FIM
FIM Study
(n=10)
AUS - 2019
All subjects followed
up to 4 years
Pivotal Study
Pivotal Study
(n=221)
US, CAN, IRE
2022-2024
​​
All subjects followed
up to 1 year
Bridging
Bridging Study
(n=40)
US, IRE - 2024
​​
All subjects followed
up to 3 months
Cross-Over
Cross-Over
Study
(n=64)
US, CAN, IRE
2022-2024​
​
Follow-up ongoing