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Data / Medical devices / Absorbent, Carbon-Dioxide

Absorbent, Carbon-Dioxide (CBL): 18 FDA-registered makers in 7 countries

18 establishments in 7 countries are registered with the FDA to make Absorbent, Carbon-Dioxide (product code CBL, Class 1, 21 CFR 868.5300). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 5 510(k) clearances under this code, the latest on October 15, 1992, and lists 5 recall events (1 Class I). FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get every maker of this deviceMakers in the United StatesWatch this device
Product code
CBL
Device class
1
Regulation
868.5300
Medical specialty
Anesthesiology

Makers by country

CountryMakers
United States5
United Kingdom4
Germany3
China3
Brazil1
Finland1
Mexico1

Makers of Absorbent, Carbon-Dioxide

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
Armstrong Medical Ltd.COLERAINE Northern Ireland, United KingdomManufacturer0011api.fda.gov
Atrasorb Industria De Produtos HospitalaresSao Roque Sao Paulo, BrazilManufacturer0000api.fda.gov
AirLife Finland OyHelsinki Uusimaa, FinlandComplaint file establishment, Specification developer0000api.fda.gov
Allied Medical LLCStuyvesant Falls, NY, United StatesManufacturer0000api.fda.gov
Draeger Safety AG & Co. KgaaLuebeck Schleswig-Holstein, GermanyContract manufacturer0000api.fda.gov
Draeger Interservices GmbHLuebeck Schleswig-Holstein, GermanyContract manufacturer0000api.fda.gov
Draegerwerk AG & Co. KGaALUEBECK Schleswig-Holstein, GermanySpecification developer0000api.fda.gov
Excellentcare Medical (Huizhou) Ltd.Huizhou Guangdong, ChinaManufacturer0000api.fda.gov
Flexicare Medical Ltd.RHONDDA CYNON TAFF Wales, United KingdomSpecification developer0000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Intersurgical Ltd.Wokingham, Berkshire, United KingdomManufacturer0000api.fda.gov
Lundell Manufacturing Corp.Minneapolis, MN, United StatesContract manufacturer0000api.fda.gov
Micropore IncElkton, MD, United StatesManufacturer0000api.fda.gov
Molecular Products IncLouisville, CO, United StatesManufacturer0000api.fda.gov
Molecular Products LtdHARLOW Essex, United KingdomManufacturer0000api.fda.gov
Productos Urologos De Mexico S.A. De C.V.MEXICALI Baja California, MexicoComplaint file establishment, Manufacturer0000api.fda.gov
Shandong Jinlai Huanhai Medical Technology Co.,ltdYantai Shandong, ChinaManufacturer0000api.fda.gov
Zhejiang Haisheng Medical Device Co., Ltd.Shaoxing Zhejiang, ChinaManufacturer0000api.fda.gov

Updated October 15, 1992. 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.