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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 3 of 7
DeviceModel / ReferenceRegistriesClassStatus
Albahealth 000868052100324
FDA UDI
Class IIActive
Albahealth C90948009990902
FDA UDI
Class IIActive
Albahealth 000768022100931
FDA UDI
Class IIActive
Albahealth 000453042100304
FDA UDI
Class IIActive
Albahealth 0N5506009990902
FDA UDI
Class IIActive
Albahealth 000853062100304
FDA UDI
Class IIActive
Albahealth 000863022100324
FDA UDI
Class IIActive
Albahealth 000863052100324
FDA UDI
Class IIActive
Albahealth 0N5507009990902
FDA UDI
Class IIActive
Albahealth 0C5589009990902
FDA UDI
Class IIActive
Albahealth 000868032100304
FDA UDI
Class IIActive
Albahealth 000473042100304
FDA UDI
Class IIActive
Albahealth 000453022100304
FDA UDI
Class IIActive
Albahealth 000853012100324
FDA UDI
Class IIActive
Albahealth 000458032100304
FDA UDI
Class IIActive
Albahealth 073004042100304
FDA UDI
Class IIActive
Albahealth 083007032100324
FDA UDI
Class IIActive
Albahealth CS5512009990304
FDA UDI
Class IIActive
Albahealth 000773022100931
FDA UDI
Class IIActive
Albahealth 000758042100931
FDA UDI
Class IIActive
Albahealth 000630009990304
FDA UDI
Class IIActive
Albahealth 083004032100324
FDA UDI
Class IIActive
Albahealth 000873032100324
FDA UDI
Class IIActive
Albahealth 0LB500012100304
FDA UDI
Class IIActive
Albahealth 000753032100931
FDA UDI
Class IIActive
Albahealth 000951042100304
FDA UDI
Class IIActive
Albahealth 000851042100324
FDA UDI
Class IIActive
Albahealth CN5507009990902
FDA UDI
Class IIActive
Albahealth 073004032100304
FDA UDI
Class IIActive
Albahealth BLS500002100304
FDA UDI
Class IIActive
Albahealth 000458022100304
FDA UDI
Class IIActive
Albahealth C20838009990304
FDA UDI
Class IIActive
Albahealth 000853032100304
FDA UDI
Class IIActive
Albahealth 091248009990902
FDA UDI
Class IIActive
Albahealth CT5412009990902
FDA UDI
Class IIActive
Albahealth C85508009990304
FDA UDI
Class IIActive
Albahealth 000568012100304
FDA UDI
Class IIActive
Albahealth 000763032100931
FDA UDI
Class IIActive
Albahealth 000868012100324
FDA UDI
Class IIActive
Albahealth 083004022100324
FDA UDI
Class IIActive
Albahealth 000468052100304
FDA UDI
Class IIActive
Albahealth 000968042100304
FDA UDI
Class IIActive
Albahealth 000473012100304
FDA UDI
Class IIActive
Albahealth 085512009990304
FDA UDI
Class IIActive
Albahealth 000953032100304
FDA UDI
Class IIActive
Albahealth 073004022100304
FDA UDI
Class IIActive
Albahealth 0N5518009990902
FDA UDI
Class IIActive
Albahealth BLS500032100304
FDA UDI
Class IIActive
Albahealth 020630009990304
FDA UDI
Class IIActive
Albahealth 0T5412009990902
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.