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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 5 of 7
DeviceModel / ReferenceRegistriesClassStatus
Albahealth BLB500022100304
FDA UDI
Class IIActive
Albahealth 0S5509009990304
FDA UDI
Class IIActive
Albahealth 0N5412009990902
FDA UDI
Class IIActive
Albahealth C91248009990902
FDA UDI
Class IIActive
Albahealth 000951022100304
FDA UDI
Class IIActive
Albahealth 000963012100304
FDA UDI
Class IIActive
Albahealth 000463052100304
FDA UDI
Class IIActive
Albahealth 000838009990304
FDA UDI
Class IIActive
Albahealth 0LS500022100304
FDA UDI
Class IIActive
Albahealth 000858012100324
FDA UDI
Class IIActive
Albahealth 000451032100304
FDA UDI
Class IIActive
Albahealth 000758022100931
FDA UDI
Class IIActive
Albahealth 000774012100931
FDA UDI
Class IIActive
Albahealth BLL500002100304
FDA UDI
Class IIActive
Albahealth 000751042100931
FDA UDI
Class IIActive
Albahealth 000868022100324
FDA UDI
Class IIActive
Albahealth 000563012100304
FDA UDI
Class IIActive
Albahealth 083004042100324
FDA UDI
Class IIActive
Albahealth 0LS500002100304
FDA UDI
Class IIActive
Albahealth 000868022100304
FDA UDI
Class IIActive
Albahealth 090630009990902
FDA UDI
Class IIActive
Albahealth 000863032100324
FDA UDI
Class IIActive
Albahealth 000973032100304
FDA UDI
Class IIActive
Albahealth 085509009990304
FDA UDI
Class IIActive
Albahealth 000773032100931
FDA UDI
Class IIActive
Albahealth 0N5508009990902
FDA UDI
Class IIActive
Albahealth 000468062100304
FDA UDI
Class IIActive
Albahealth 090948009990902
FDA UDI
Class IIActive
Albahealth CN5512009990902
FDA UDI
Class IIActive
Albahealth 000753012100931
FDA UDI
Class IIActive
Albahealth 000958032100304
FDA UDI
Class IIActive
Albahealth 000563022100304
FDA UDI
Class IIActive
Albahealth 083007012100304
FDA UDI
Class IIActive
Albahealth 000558022100304
FDA UDI
Class IIActive
Albahealth 000851012100304
FDA UDI
Class IIActive
Albahealth 000958042100304
FDA UDI
Class IIActive
Albahealth 000853052100304
FDA UDI
Class IIActive
Albahealth 000851042100304
FDA UDI
Class IIActive
Albahealth 083007042100304
FDA UDI
Class IIActive
Albahealth 000858032100324
FDA UDI
Class IIActive
Albahealth 000873012100324
FDA UDI
Class IIActive
Albahealth BLS500012100304
FDA UDI
Class IIActive
Albahealth 053558012100304
FDA UDI
Class IIActive
Albahealth 000958022100304
FDA UDI
Class IIActive
Albahealth 073007012100304
FDA UDI
Class IIActive
Albahealth 000573012100304
FDA UDI
Class IIActive
Albahealth 000751052100931
FDA UDI
Class IIActive
Albahealth C85507009990304
FDA UDI
Class IIActive
Albahealth 000953012100304
FDA UDI
Class IIActive
Albahealth 0S5012009990304
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.