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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 2 of 7
DeviceModel / ReferenceRegistriesClassStatus
Albahealth 073007022100304
FDA UDI
Class IIActive
Albahealth 053558G22100304
FDA UDI
Class IIActive
Albahealth 000463022100304
FDA UDI
Class IIActive
Albahealth 000958052100304
FDA UDI
Class IIActive
Albahealth 0LF700022100304
FDA UDI
Class IIActive
Albahealth CT5636009990902
FDA UDI
Class IIActive
Albahealth C90630009990902
FDA UDI
Class IIActive
Albahealth CN5506009990902
FDA UDI
Class IIActive
Albahealth 000853062100324
FDA UDI
Class IIActive
Albahealth 000973012100304
FDA UDI
Class IIActive
Albahealth 059001023680304
FDA UDI
Class IIActive
Albahealth 083007042100324
FDA UDI
Class IIActive
Albahealth CN5012009990902
FDA UDI
Class IIActive
Albahealth 000775022100931
FDA UDI
Class IIActive
Albahealth 000451042100304
FDA UDI
Class IIActive
Albahealth 059001033690304
FDA UDI
Class IIActive
Albahealth 000758052100931
FDA UDI
Class IIActive
Albahealth 083004042100304
FDA UDI
Class IIActive
Albahealth 000968022100304
FDA UDI
Class IIActive
Albahealth 000474052100304
FDA UDI
Class IIActive
Albahealth 000968012100304
FDA UDI
Class IIActive
Albahealth C85530009990304
FDA UDI
Class IIActive
Albahealth 000858032100304
FDA UDI
Class IIActive
Albahealth 000853042100324
FDA UDI
Class IIActive
Albahealth 000751012100931
FDA UDI
Class IIActive
Albahealth 000873012100304
FDA UDI
Class IIActive
Albahealth 0N5530009990902
FDA UDI
Class IIActive
Albahealth 021048009990304
FDA UDI
Class IIActive
Albahealth 000958012100304
FDA UDI
Class IIActive
Albahealth BLS500022100304
FDA UDI
Class IIActive
Albahealth 000458042100304
FDA UDI
Class IIActive
Albahealth 000868032100324
FDA UDI
Class IIActive
Albahealth 0N5564009990902
FDA UDI
Class IIActive
Albahealth BLF700012100304
FDA UDI
Class IIActive
Albahealth C01048009990304
FDA UDI
Class IIActive
Albahealth 073007032100304
FDA UDI
Class IIActive
Albahealth 000951012100304
FDA UDI
Class IIActive
Albahealth BLL500012100304
FDA UDI
Class IIActive
Albahealth 000753042100931
FDA UDI
Class IIActive
Albahealth 0LS500012100304
FDA UDI
Class IIActive
Albahealth 000751032100931
FDA UDI
Class IIActive
Albahealth B53558G22100304
FDA UDI
Class IIActive
Albahealth 000863032100304
FDA UDI
Class IIActive
Albahealth 000963042100304
FDA UDI
Class IIActive
Albahealth 000463012100304
FDA UDI
Class IIActive
Albahealth C91048009990902
FDA UDI
Class IIActive
Albahealth 000573042100304
FDA UDI
Class IIActive
Albahealth 000463042100304
FDA UDI
Class IIActive
Albahealth 0N5538009990902
FDA UDI
Class IIActive
Albahealth 000953022100304
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.