Anscare LeniScar Silicone Stick

FDA UDI

Class I (US FDA UDI)

by Benq Materials Corp.

Identity

Trade Name: Anscare LeniScar Silicone Stick FDA UDI
Generic Name: Scar-management dressing, reusable FDA UDI
Device Name: Anscare Leniscar Silicone Stick provides an easy-to-use topical scar treatment. It is intended to diminish hypertrophic scars and keloids characterized with a raised or discolored appearance. LeniScar is an advanced silicone formula which contains medical grade silicone and antioxidant vitamin C & E. It creates a waterproof, transparent thin film which helps to maintain the moisture balance of skin and provides an optimal protective barrier for the scar to restore. FDA UDI
Model / Reference: SP-200-1 FDA UDI
Description: Anscare Leniscar Silicone Stick provides an easy-to-use topical scar treatment. It is intended to diminish hypertrophic scars and keloids characterized with a raised or discolored appearance. LeniScar is an advanced silicone formula which contains medical grade silicone and antioxidant vitamin C & E. It creates a waterproof, transparent thin film which helps to maintain the moisture balance of skin and provides an optimal protective barrier for the scar to restore. FDA UDI

Identifiers

Primary DI / UDI-DI: 04719745504525 FDA UDI
FDA Product Code: MDA FDA UDI
GMDN Term: Scar-management dressing, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4025 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Scar-management dressing, reusable

Anscare LeniScar Silicone Stick by Benq Materials Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Benq Materials Corp.

Sources (1)

FDA UDI b6180e3c-765c-490a-b74d-c322588c7b1e 33 fields · synced May 30, 2026