710 Allure 711P

No FDA recalls on record, checked 23 Oct 2026.

Trade Name

710 Allure

Generic Name

Compression/pressure sock/stocking, single-use

Model / Ref / Catalog

711P, 711PMLW19

Primary DI / UDI-DI

00745129265199

FDA Product Code

FQL

GMDN Term

Compression/pressure sock/stocking, single-use

Device Class

Class I

Regulation Number

880.5780

GUDID distribution status

Not in Commercial Distribution

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See all devices from Sigvaris, Inc. →