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Companies / Lavior Pharma
Medical device company profile

Lavior Pharma

Florida medical device developer and brand owner of botanical hydrogel wound dressings and skin barrier products.

Medical Device Developer and ManufacturerGeneral Medical & Patient CareWound Care
HeadquartersπŸ‡ΊπŸ‡ΈHallandale Beach, Florida, United States
Founded2010
Commercial statusCommercially availableCommercial hydrogel wound dressings and skin barrier products.
Employees11–50 [18]LinkedIn company-size range Β· Checked 2026-11-03
Estimated revenueNot confirmed
Official websitelavior.com β†—

Company overview

Lavior Pharma develops and markets botanical wound-care and skin-barrier products for consumers and healthcare professionals. Founded in 2010 by Gilad and Anabelle Savion, the Florida company is led by Gilad as CEO and Anabelle as COO. Its registered business address is in Hallandale Beach.

The range combines hydrogel formulations with the company’s AGS-RIED botanical extract from Inula viscosa. Lavior describes control of cultivation, harvesting and extraction and markets its products as made in the USA. FDA lists the company as a specification developer for the hydrogel range. Consumer tubes and larger professional formats serve wound-care practices, distributors and home-care users.

A 65-patient randomized study published in the Journal of Wound Care in July 2025 compared Lavior Diabetic Wound Gel with SoloSite. It reported comparable wound-closure times, with improvements in some patient-reported measures. Lavior also partners with Lovell Government Services to expand access through federal healthcare procurement channels.

[7][9][14][16][17][18][19]

Leadership

3 people
Gilad SavionCo-founder & Chief Executive Officer [7]
Anabelle SavionCo-founder & Chief Operating Officer [7]
Mary E. Hanley, DOChief Medical Officer [7]

Products & regulatory status How does MedTechIndex get this information?

Summary

FDA lists Lavior Pharma as a specification developer for its hydrogel wound-dressing and barrier-care range. The listed NAE category is Class I and exempt from 510(k) premarket notification. Current product records identify the diabetic wound hydrogel, multipurpose wound gel, post-surgical barrier gel and diabetic skin barrier cream under this category; these are device listings, rather than individual FDA clearance decisions. [17][15][1][2][4][3]

Current labeling separates wound moisture management from care of closed incisions and dry, intact skin. The Diabetic Skin Barrier Cream is specifically described as a non-medicated skin-care product, not a treatment for open wounds. Professional β€œAdvanced” tubes and consumer tubes are marketed in different sizes within the respective product lines. [6][13][9]

Regulatory snapshot How to read this snapshot

U.S. FDA
β€”
510(k) clearances
β€”
De Novo grants
β€”
PMA approvals
β€”
Recall events

Latest recorded source review: 2026-11-03.

Scope: selected product families.

Commercial portfolio snapshot

Documented commercial product families.

Lavior Diabetic Wound Hydrogel official product tube
Image: Lavior Pharma
Hydrogel wound dressing

Diabetic Wound Hydrogel β†—

Botanical hydrogel dressing designed to maintain a moist wound environment. The range includes a 1 fl oz consumer tube and the 3 fl oz Advanced Diabetic Wound Hydrogel for professional supply. [10][1][17]

Commercially available Β· Listed exempt device family
Lavior Post-Surgical / Advanced Post-Procedure Barrier Gel official product tube
Image: Lavior Pharma
Skin barrier gel

Post-Surgical / Advanced Post-Procedure Barrier Gel β†—

Gel for protecting and moisturizing recovering skin after procedures. The consumer product is directed to closed incisions; a 3 fl oz Advanced Post-Procedure Skin Barrier Gel is offered to professionals. [12][4][17]

Commercially available Β· Listed exempt device family
Lavior Diabetic Skin Barrier Cream official product tube
Image: Lavior Pharma
Non-medicated skin barrier cream

Diabetic Skin Barrier Cream β†—

Daily-use cream for dry, intact skin, including feet, legs and hands. It is separate from the wound hydrogel range and is not intended for open wounds. [13][3][17]

Commercially available Β· Listed exempt device family

Activity & Milestones

3 events
2026-06-23 Β· Commercial

Federal healthcare access partnership announced

Lavior and Lovell Government Services announced a partnership serving federal healthcare procurement channels. [19]

2025-07-01 Β· Clinical

Randomized hydrogel study published

Journal of Wound Care published a six-week comparison involving 65 patients. Wound-closure times were comparable between groups. [14]

2010 Β· Company

Lavior founded

Gilad and Anabelle Savion founded the business. [7]

19 Cited Sources

Accessed 11/03/2026

Last substantive review: 11/3/2026

[1] Diabetic Wound Hydrogel β€” device model DWG10US1 β†—U.S. National Library of Medicine / FDA Β· regulatory
[2] Multipurpose Wound Gel β€” device model MWG10US1 β†—U.S. National Library of Medicine / FDA Β· regulatory
[3] Diabetic Skin Barrier Cream β€” device model DSB34US1 β†—U.S. National Library of Medicine / FDA Β· regulatory
[4] Post-Surgical Skin Barrier Gel β€” device model PSG10US1 β†—U.S. National Library of Medicine / FDA Β· regulatory
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