Philips Image Guided Therapy Corporation
12 product lines across 3 device categories: Atherectomy, Drug-coated balloons, Guidewires.
From philips.com, checked October 2026.
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About Philips Image Guided Therapy Corporation
Philips Image Guided Therapy Corporation hasn't added a company description yet.
Atherectomy Devices
Used in: Peripheral Atherectomy
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Phoenix 2.2mm x 130cm 6F Atherectomy System | Outer Diameter: 1.5–2.2 mm; Length: 130–149 cm | 5 | Not stated |
| Phoenix 2.2mm x 149cm 6F Atherectomy Catheter | Outer Diameter: 1.5–2.2 mm; Length: 130–149 cm | 5 | Not stated |
| Turbo-Power Laser Atherectomy Catheter Turbo-Power Laser Atherectomy Catheter, 2.0mm | Catheter Working Length: 125–150 cm | 2 | Not stated |
| Phoenix 2.2mm x 130cm 6F Pre-Deflected Atherectomy System | Outer Diameter: 2.2–2.4 mm; Length: 130 cm | 2 | Not stated |
| Phoenix 2.2mm x 130cm 6F Pre-Deflected Atherectomy Catheter | Outer Diameter: 2.2–2.4 mm; Length: 130 cm | 2 | Not stated |
Drug-Coated Balloons
Used in: Peripheral Balloon Angioplasty, Peripheral Atherectomy
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Stellarex 0.035" OTW drug-coated angioplasty balloon 4mm x 40mm x 80cm | Balloon Diameter: 4–6 mm; Balloon Length: 40–200 mm; Catheter Length: 80–135 cm | 42 | Not stated |
| Stellarex Stellarex 0.035 OTW Drug-coated Angioplasty Balloon (5mm x 100mm) x 135cm | Balloon Diameter: 4–6 mm; Balloon Length: 40–200 mm; Catheter Length: 80–135 cm | 42 | Not stated |
Guidewires
Used in: Uterine Artery Embolization (UAE), Peripheral Balloon Angioplasty, Stroke Thrombectomy, Internal Iliac Artery Embolization
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Verrata Plus Pressure Guide Wire | Outer Diameter: 0.01 in; Length: 185–300 cm | 4 | Not stated |
| FloWire Doppler Guide Wire | — | 3 | Not stated |
| OmniWire Pressure guide wire | Outer Diameter: 0.01 in; Length: 185 cm | 2 | MR Unsafe |
| Phoenix Floppy Tip, Light Support Guidewire Phoenix 0.014" Guidewire | — | 1 | Not stated |
| Phoenix Floppy Tip, Extra Support Guidewire 0.014" guidewire | — | 1 | Not stated |
Sales representatives
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From philips.com, checked October 2026.
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FDA clearances and approvals
- turbo-power 2 0mm laser atherectomy catheters turbo-power 2 3mm laser atherectomy catheters 510K K222837, 2022
- 2 4mm x 130cm phoenix deflecting atherectomy system 1 5mm x 149cm phoenix atherectomy system 510K K211518, 2021
- stellarex 0 035 otw drug-coated angioplasty ballon PMA P160049, 2019
- phoenix atherectomy system 510K K182972, 2018
- 1 8mm x 149 cm phoenix atherectomy catheter 2 2mm x 149 cm phoenix atherectomy catheter phoenix handle phoenix wire support clip 510K K143328, 2014
- 1 8 mm phoenix atherectomy catheter 2 2 mm phoenix atherectomy catheter phoenix handle phoenix wire support clip 510K K140944, 2014
Frequently asked questions
What devices does Philips Image Guided Therapy Corporation make?
Philips Image Guided Therapy Corporation has 12 product lines in our library across 3 device categories: Atherectomy, Drug-coated balloons, Guidewires.
Are Philips Image Guided Therapy Corporation devices FDA cleared?
Our library lists FDA clearances and approvals for Philips Image Guided Therapy Corporation products. The most recent is turbo-power 2 0mm laser atherectomy catheters turbo-power 2 3mm laser atherectomy catheters (510(k) K222837, 2022).
How do I contact a Philips Image Guided Therapy Corporation sales representative?
Philips Image Guided Therapy Corporation has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.
Does LA Vascular sell Philips Image Guided Therapy Corporation products?
No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Philips Image Guided Therapy Corporation or its representatives to buy.
Where do the Philips Image Guided Therapy Corporation product sizes come from?
From the FDA Global Unique Device Identification Database (GUDID). Confirm sizes and availability with the instructions for use or the manufacturer.
Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.