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XprESS ENT dilation system
The XprESS ENT dilation system delivers a unique combination of control and versatility for ENT balloon dilation. Its familiar seeker-based design and tip malleability provide the tactile feel you are accustomed to and the flexibility you need to address both chronic rhinosinusitis or Eustachian tube dysfunction patients.1-2
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The XprESS ENT dilation system offers surgeons a unique set of features and benefits.1 These features include:
- A slim profile that enables easy visualization, access and navigation of narrow anatomy
- The integrated Path Assist LED light fiber delivers light confirmation through trans-illumination and excursion, eliminating the need for an extra light source and cables
- Malleable tip that allows for customization based on patient anatomy to treat the frontal, maxillary, sphenoid sinuses and the eustachian tube
- Compatible with the Stryker ENT navigation system, allowing for navigated confirmation*
- Compact balloon sizes for use across patient populations including pediatrics
*The XprESS LoProfile dilation device is trackable with the Stryker ENT navigation system during balloon sinus dilation procedures, when used with the TGS guidewire
550K
patients treated4
8
clinical trials
98%
technical success rate5
~0.07%
complication rate4
Proven patient outcomes
3x
Faster*
Return to normal activities
with BSD vs. ESS6
* in adult patients
≤1.4%
Revision rate*
At 1 year post-procedure5,7
* in adult patients
>96% Patency*
At 1 year post-procedure8
* in adult patients
4 out of 5 Responders*
SNOT-20 improvement at 1 year8
* in adult patients
1 | Designed for performance
Ergonomically engineered to fit naturally in your hand, XprESS enables one-finger advancement while supporting your technique for stability, control and precise positioning in procedures.9
2 | Compact design
A slim, 1.25mm profile enables easy visualization and precise access in narrow and pediatric anatomy.¹
3 | Light confirmation
Integrated Path Assist LED light fiber delivers light confirmation through trans-illumination and excursion, eliminating the need for an extra light source and cables.
4 | Tactile feel
Malleable, seeker-based tip inspired by traditional ENT instruments designed to support precise placement and atraumatic navigation.
5 | Distal markers
1cm and 2cm depth markings provide visual cues on placement.
The XprESS instrument technology is designed for both office and OR procedures. XprESS takes inspiration from traditional ENT tools and other FESS instruments, such as the frontal seeker, frontal curette, olive tip probe and double ball probe. The slim profile of the XprESS device is designed to enable easy endoscopic visualization and placement of the device.
Distal markers
1 and 2 cm reference markings provide visual cue on placement position.
Tactile feel
Provides healthcare provider confidence and control to access the sinus.1
Light illumination
Leverage light confirmation* to confirm access.1
*Using the PathAssist LED light fiber packaged with the XprESS ENT dilation system
Light and Excursion
For frontal and maxillary dilations, leverage medial to lateral excursion.
Dependable tracking*
Trackable with the Stryker ENT navigation system when used with a TGS guidewire and the XprESS LoPro Balloon Dilation System1,3
*The XprESS LoProfile dilation device is trackable with the Stryker ENT navigation system during balloon sinus dilation procedures, when used with the TGS guidewire
Visualization
The sleek profile design allows for endoscopic visualization of treatment areas
A balloon sinuplasty device in the office. A tool for hybrid FESS cases in the OR. One versatile device designed to support your technique—product options include:
| Product | Ordering no. | Description |
| XprESS LoProfile system | LPLF-106 | 6 x 20 mm, 1 system |
| XprESS LoProfile system | LPLF-107 | 7 x 20 mm, 1 system |
| XprESS LoProfile system | LPLF-205 | 5 x 8 mm, 1 system |
| XprESS LoProfile system | LPLF-206 | 6 x 8 mm, 1 system |
| XprESS Ultra system | ULF-106 | 6 x 20 mm, 1 system |
| XprESS Ultra system | ULF-206 | 6 x 8 mm, 1 system |
One system includes: 1 balloon dilation device, 1 inflation syringe, 1 extension line, 1 bending tool, 1 PathAssist LED light fiber
Reinforced anesthesia needle
Audion® ET dilation system
Stryker ENT navigation system
Questions about XprESS or
balloon dilation products?
Thank you!
References
- XprESS Instructions for use 4322-001
- Data on file at Stryker DHF 1656-001
- TGS guidewire instructions for use 5176-001
- Internal data on file
- Chandra, R. K., Kern, R. C., Cutler, J. L., Welch, K. C., & Russell, P. T. (2016). REMODEL larger cohort with long-term outcomes and meta-analysis of standalone balloon dilation studies. The Laryngoscope, 126(1), 44–50. https://doi.org/10.1002/lary.25507
- Cutler, J., Bikhazi, N., Light, J., Truitt, T., Schwartz, M., Armstrong, M., Bikhazi, N., Chandler, S., Cutler, J., Ferouz-Colborn, A., Gould, J., Light, J., Marvel, J., Schwartz, M., & Truitt, T. (2013). Standalone Balloon Dilation versus Sinus Surgery for Chronic Rhinosinusitis: A Prospective, Multicenter, Randomized, Controlled Trial. American Journal of Rhinology & Allergy, 27(5), 416–422. https://doi.org/10.2500/ajra.2013.27.3970
- Gould, J., Alexander, I., Tomkin, E., & Brodner, D. (2014). In-Office, Multisinus Balloon Dilation: 1-Year Outcomes from a Prospective, Multicenter, Open Label Trial. American Journal of Rhinology & Allergy, 28(2), 156–163. https://doi.org/10.2500/ajra.2014.28.4043
- Bikhazi, N., Light, J., Truitt, T., Schwartz, M., Cutler, J., & Investigators, R. S. (2014). Standalone balloon dilation versus sinus surgery for chronic rhinosinusitis: A prospective, multicenter, randomized, controlled trial with 1-year follow-up. American Journal of Rhinology & Allergy, 28(4), 323–329. https://doi.org/10.2500/ajra.2014.28.4064
- D0000397950 - Internal data on file
Disclaimer
This document is intended solely for the use of healthcare professionals. A surgeon must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. We do not dispense medical advice and recommend that surgeons be trained in the use of any particular product before using it in surgery.
A physician using XprESS for Eustachian tube dilation must either have: (i) experience with a Eustachian tube balloon dilation device or (ii) undergone cadaver training on the use of a balloon dilation device for Eustachian tube dilation.
If a physician who intends to use XprESS for Eustachian tube dilation does not meet at least one of these criteria, please contact your Stryker representative to arrange training
The information presented is intended to demonstrate Stryker’s products. A surgeon must always refer to the package insert, product label and/or instructions for use, including the instructions for cleaning and sterilization (if applicable), before using any of Stryker’s products. Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets. Please contact your representative if you have questions about the availability of Stryker’s products in your area.
Stryker or its affiliated entities own, use, or have applied for the following trademarks or service marks: TGS, XprESS and Stryker. All other trademarks are trademarks of their respective owners or holders. The absence of a product, feature, or service name, or logo from this list does not constitute a waiver of Stryker’s trademark or other intellectual property rights concerning that name or logo.
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