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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 4 of 7
DeviceModel / ReferenceRegistriesClassStatus
Albahealth 000775032100931
FDA UDI
Class IIActive
Albahealth BLB500032100304
FDA UDI
Class IIActive
Albahealth 000863052100304
FDA UDI
Class IIActive
Albahealth BLL500022100304
FDA UDI
Class IIActive
Albahealth CN5530009990902
FDA UDI
Class IIActive
Albahealth 073007042100304
FDA UDI
Class IIActive
Albahealth 000953042100304
FDA UDI
Class IIActive
Albahealth 000468022100304
FDA UDI
Class IIActive
Albahealth 000573052100304
FDA UDI
Class IIActive
Albahealth 000858022100304
FDA UDI
Class IIActive
Albahealth 000973052100304
FDA UDI
Class IIActive
Albahealth 000863012100324
FDA UDI
Class IIActive
Albahealth 000973022100304
FDA UDI
Class IIActive
Albahealth 000853052100324
FDA UDI
Class IIActive
Albahealth 0S5512009990304
FDA UDI
Class IIActive
Albahealth 059001023690304
FDA UDI
Class IIActive
Albahealth 000858052100324
FDA UDI
Class IIActive
Albahealth 0LB500032100304
FDA UDI
Class IIActive
Albahealth 000951052100304
FDA UDI
Class IIActive
Albahealth CN5509009990902
FDA UDI
Class IIActive
Albahealth 000851032100304
FDA UDI
Class IIActive
Albahealth CN5416009990902
FDA UDI
Class IIActive
Albahealth 000873042100304
FDA UDI
Class IIActive
Albahealth CS5509009990304
FDA UDI
Class IIActive
Albahealth CT5012009990902
FDA UDI
Class IIActive
Albahealth 000453062100304
FDA UDI
Class IIActive
Albahealth 000868042100324
FDA UDI
Class IIActive
Albahealth 000868052100304
FDA UDI
Class IIActive
Albahealth 000758032100931
FDA UDI
Class IIActive
Albahealth 000863042100324
FDA UDI
Class IIActive
Albahealth 000873032100304
FDA UDI
Class IIActive
Albahealth 083007022100324
FDA UDI
Class IIActive
Albahealth 000851032100324
FDA UDI
Class IIActive
Albahealth 000858042100304
FDA UDI
Class IIActive
Albahealth 000968032100304
FDA UDI
Class IIActive
Albahealth 000773012100931
FDA UDI
Class IIActive
Albahealth 0T5509009990902
FDA UDI
Class IIActive
Albahealth 000953062100304
FDA UDI
Class IIActive
Albahealth BLB500002100304
FDA UDI
Class IIActive
Albahealth 000873022100304
FDA UDI
Class IIActive
Albahealth 0M5108009990902
FDA UDI
Class IIActive
Albahealth 000963052100304
FDA UDI
Class IIActive
Albahealth 000451022100304
FDA UDI
Class IIActive
Albahealth 000453052100304
FDA UDI
Class IIActive
Albahealth 000863012100304
FDA UDI
Class IIActive
Albahealth 000573022100304
FDA UDI
Class IIActive
Albahealth CN5504009990902
FDA UDI
Class IIActive
Albahealth B53558G12100304
FDA UDI
Class IIActive
Albahealth 000873022100324
FDA UDI
Class IIActive
Albahealth 0N5408009990902
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.