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Albahealth, LLC

US

Last updated May 23, 2026

What Albahealth, LLC makes

Albahealth, LLC produces single-use compression garments, including pressure socks and stockings designed for venous support, as well as multi-chamber venous compression systems. They also manufacture single-use patient surgical drapes intended for sterile barrier protection during medical procedures.

The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) database. Albahealth, LLC operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
003375805

Catalogue (304)

Page 1 of 7
DeviceModel / ReferenceRegistriesClassStatus
Albahealth 000863022100304
FDA UDI
Class IIActive
Albahealth 000858012100304
FDA UDI
Class IIActive
Albahealth 083004012100304
FDA UDI
Class IIActive
Albahealth 000453012100304
FDA UDI
Class IIActive
Albahealth 085507009990304
FDA UDI
Class IIActive
Albahealth 000973042100304
FDA UDI
Class IIActive
Albahealth 073004012100304
FDA UDI
Class IIActive
Albahealth 000953052100304
FDA UDI
Class IIActive
Albahealth BLL500032100304
FDA UDI
Class IIActive
Albahealth 000473022100304
FDA UDI
Class IIActive
Albahealth 000858022100324
FDA UDI
Class IIActive
Albahealth 000851022100304
FDA UDI
Class IIActive
Albahealth BLB500012100304
FDA UDI
Class IIActive
Albahealth 000451012100304
FDA UDI
Class IIActive
Albahealth 000468012100304
FDA UDI
Class IIActive
Albahealth 000963032100304
FDA UDI
Class IIActive
Albahealth CS5012009990304
FDA UDI
Class IIActive
Albahealth 000868062100304
FDA UDI
Class IIActive
Albahealth 0T5012009990902
FDA UDI
Class IIActive
Albahealth 000853012100304
FDA UDI
Class IIActive
Albahealth 0LL500012100304
FDA UDI
Class IIActive
Albahealth 000853042100304
FDA UDI
Class IIActive
Albahealth CN5412009990902
FDA UDI
Class IIActive
Albahealth 053558022100304
FDA UDI
Class IIActive
Albahealth 000451052100304
FDA UDI
Class IIActive
Albahealth 000763022100931
FDA UDI
Class IIActive
Albahealth CT5507009990902
FDA UDI
Class IIActive
Albahealth 0T5512009990902
FDA UDI
Class IIActive
Albahealth 0LS500032100304
FDA UDI
Class IIActive
Albahealth B53558022100304
FDA UDI
Class IIActive
Albahealth 090838009990902
FDA UDI
Class IIActive
Albahealth 000568032100304
FDA UDI
Class IIActive
Albahealth 083007022100304
FDA UDI
Class IIActive
Albahealth 000558042100304
FDA UDI
Class IIActive
Albahealth C21048009990304
FDA UDI
Class IIActive
Albahealth B53558012100304
FDA UDI
Class IIActive
Albahealth 000863042100304
FDA UDI
Class IIActive
Albahealth 083004012100324
FDA UDI
Class IIActive
Albahealth C85512009990304
FDA UDI
Class IIActive
Albahealth 083004022100304
FDA UDI
Class IIActive
Albahealth 085508009990304
FDA UDI
Class IIActive
Albahealth C85509009990304
FDA UDI
Class IIActive
Albahealth 000473052100304
FDA UDI
Class IIActive
Albahealth C90838009990902
FDA UDI
Class IIActive
Albahealth 000968062100304
FDA UDI
Class IIActive
Albahealth 000873042100324
FDA UDI
Class IIActive
Albahealth 0LL500032100304
FDA UDI
Class IIActive
Albahealth 000775012100931
FDA UDI
Class IIActive
Albahealth 000853032100324
FDA UDI
Class IIActive
Albahealth 0LF700012100304
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Albahealth, LLC has one FDA recall record initiated on 2011-10-12, which is listed with a terminated status. The recall was due to the wrap portion of the device tearing at the seam.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Oct 12, 2011Z-0183-2012—terminated

The wrap portion of the device was tearing at the seam.