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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 6 of 7
DeviceModel / ReferenceRegistriesClassStatus
Albahealth 000753062100931
FDA UDI
Class IIActive
Albahealth 000553042100304
FDA UDI
Class IIActive
Albahealth 059001013690304
FDA UDI
Class IIActive
Albahealth 000873052100324
FDA UDI
Class IIActive
Albahealth 059001033680304
FDA UDI
Class IIActive
Albahealth 0LB500002100304
FDA UDI
Class IIActive
Albahealth 000868062100324
FDA UDI
Class IIActive
Albahealth 000563032100304
FDA UDI
Class IIActive
Albahealth 0N5509009990902
FDA UDI
Class IIActive
Albahealth 0LL500022100304
FDA UDI
Class IIActive
Albahealth 000558012100304
FDA UDI
Class IIActive
Albahealth 020838009990304
FDA UDI
Class IIActive
Albahealth CT5509009990902
FDA UDI
Class IIActive
Albahealth 083007012100324
FDA UDI
Class IIActive
Albahealth 053558C22100304
FDA UDI
Class IIActive
Albahealth 053558G12100304
FDA UDI
Class IIActive
Albahealth 0N5512009990902
FDA UDI
Class IIActive
Albahealth 000868042100304
FDA UDI
Class IIActive
Albahealth CN5508009990902
FDA UDI
Class IIActive
Albahealth 0LL500002100304
FDA UDI
Class IIActive
Albahealth BLF700022100304
FDA UDI
Class IIActive
Albahealth 000968052100304
FDA UDI
Class IIActive
Albahealth 000773042100931
FDA UDI
Class IIActive
Albahealth 000851052100324
FDA UDI
Class IIActive
Albahealth 083007032100304
FDA UDI
Class IIActive
Albahealth 000858052100304
FDA UDI
Class IIActive
Albahealth 000568022100304
FDA UDI
Class IIActive
Albahealth 000553032100304
FDA UDI
Class IIActive
Albahealth CN5518009990902
FDA UDI
Class IIActive
Albahealth 0N5416009990902
FDA UDI
Class IIActive
Albahealth 000458052100304
FDA UDI
Class IIActive
Albahealth 059001013680304
FDA UDI
Class IIActive
Albahealth CN5408009990902
FDA UDI
Class IIActive
Albahealth 000768012100931
FDA UDI
Class IIActive
Albahealth 000963022100304
FDA UDI
Class IIActive
Albahealth 000753052100931
FDA UDI
Class IIActive
Albahealth 000751022100931
FDA UDI
Class IIActive
Albahealth CN5536009990902
FDA UDI
Class IIActive
Albahealth 000858042100324
FDA UDI
Class IIActive
Albahealth 000868012100304
FDA UDI
Class IIActive
Albahealth C20630009990304
FDA UDI
Class IIActive
Albahealth 000951032100304
FDA UDI
Class IIActive
Albahealth CT5512009990902
FDA UDI
Class IIActive
Albahealth 000851012100324
FDA UDI
Class IIActive
Albahealth 000873052100304
FDA UDI
Class IIActive
Albahealth 000853022100324
FDA UDI
Class IIActive
Albahealth 0C5569009990902
FDA UDI
Class IIActive
Albahealth 083004032100304
FDA UDI
Class IIActive
Albahealth 091048009990902
FDA UDI
Class IIActive
Albahealth 000553012100304
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.