InnovaMatrix® FS
InnovaMatrix® FS is designed to help manage exudate. InnovaMatrix® FS is part of the InnovaMatrix® family of products that are the only placental-derived ECM medical devices cleared by the FDA for wound management.
InnovaMatrix® FS is a placental-derived device that preserves the inherent structural benefits of the placenta while adding the reliability, reproducibility, and safety profile of a medical device.1,2,3
InnovaMatrix® FS requires no product preparation prior to placement on a wound, no specific orientation for placement, and no tissue tracking.
Indicated for the management of wounds including*:
- Partial and full-thickness wounds
- Pressure ulcers
- Venous ulcers
- Diabetic ulcers
- Chronic vascular ulcers
- Tunneled/undermined wounds
- Surgical wounds (donor sites/grafts, post-Mohs surgery, post- laser surgery, podiatric, wound dehiscence)
- Trauma wounds (abrasions, lacerations, and skin tears)
- Partial-thickness second degree burns
- Draining wounds
The device is intended for one-time use.
Available Sizes
Part # |
Size |
|
IMF-0202-01 |
Fenestrated Placental ECM 2cm x 2cm |
|
IMF-0404-01 |
Fenestrated Placental ECM 4cm x 4cm |
|
IMBF-0505-01 |
Fenestrated Placental ECM 5cm x 5cm |
Contraindications
This device is derived from porcine collagen and should not be used on patients with sensitivity or
allergy to porcine materials; sensitivity or allergy to collagen; or active or latent infection in or around
the application site.
This device is not indicated for use in third degree burns.
Coverage and Reimbursement Support
We partner with our customers to provide reimbursement support, including insurance verifications,
payor trends, and claims and prior authorization support.
Need Help?
Contact us: 888-767-4849 or reimbursement.wound@convatec.com
Request a sample of our product
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References
*See package insert for full list of indications.
- RDR-002
- Badylak MEMO-001
- K193552 510(k) Summary