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Data / Medical devices / Warmer, Irrigation Solution

Warmer, Irrigation Solution (LHC): 21 FDA-registered makers in 6 countries

21 establishments in 6 countries are registered with the FDA to make Warmer, Irrigation Solution (product code LHC, Class 1, 21 CFR 890.5950). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 24 510(k) clearances under this code, the latest on June 7, 2016, and lists 3 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
LHC
Device class
1
Regulation
890.5950
Medical specialty
Physical Medicine

Makers by country

CountryMakers
United States15
India2
Dominican Republic1
China1
Belgium1
Turkey1

Makers of Warmer, Irrigation Solution

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Mac MedicalMillstadt, IL, United StatesContract manufacturer, Manufacturer, Remanufacturer1June 13, 2008000api.fda.gov
Blickman Industries LLCLawrenceburg, TN, United StatesRemanufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Currie Medical, Inc.Franklin, TN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Currie Medical, Inc.Norfolk, VA, United StatesManufacturer, Remanufacturer, Specification developer0000api.fda.gov
Das Medical International, SRLLa Romana, Dominican RepublicContract manufacturer0000api.fda.gov
Dongguan Hong De Medical Plastic Products Co. Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Genadyne Biotechnologies, Inc.Hicksville, NY, United StatesManufacturer for export0000api.fda.gov
Haywood Vocational Opportunities Inc.Waynesville, NC, United StatesContract manufacturer0000api.fda.gov
Mark EnterprisesNashik Maharashtra, IndiaManufacturer0000api.fda.gov
Marken Healthtech LimitedNASHIK Maharashtra, IndiaManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
MFG One, LLCChantilly, VA, United StatesContract manufacturer0000api.fda.gov
Microtek Medical LLCEagan, MN, United StatesSpecification developer0000api.fda.gov
Microtek Medical LLCNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Microtek Medical LLCAlpharetta, GA, United StatesSpecification developer0000api.fda.gov
Orfit Industries NVWIJNEGEM Antwerpen, BelgiumManufacturer0000api.fda.gov
Pedigo Products, Inc.Vancouver, WA, United StatesManufacturer0000api.fda.gov
Rac Medical SolutionsBruceton, TN, United StatesManufacturer0000api.fda.gov
Sumer Uluslararasi San. Ve Tic. A.S.Sincan Ankara, TurkeyManufacturer0000api.fda.gov
Tryptech ServicesGreensboro, NC, United StatesManufacturer0000api.fda.gov
WEG Surgical SolutionsGreensboro, NC, United StatesSpecification developer0000api.fda.gov

Updated June 7, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.