Data / Medical devices / Monitor, Carbon-Dioxide, Cutaneous
Monitor, Carbon-Dioxide, Cutaneous (LKD): 13 FDA-registered makers in 7 countries
13 establishments in 7 countries are registered with the FDA to make Monitor, Carbon-Dioxide, Cutaneous (product code LKD, Class 2, 21 CFR 868.2480). 5 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 17 510(k) clearances under this code, the latest on May 17, 2024, and lists 15 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- LKD
- Device class
- 2
- Regulation
- 868.2480
- Medical specialty
- Anesthesiology
Makers by country
| Country | Makers |
|---|---|
| Germany | 3 |
| United States | 3 |
| Switzerland | 2 |
| Poland | 2 |
| Sweden | 1 |
| Denmark | 1 |
| China | 1 |
Makers of Monitor, Carbon-Dioxide, Cutaneous
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.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Sentec AG | THERWIL Basel-Landschaft, Switzerland | Contract manufacturer, Manufacturer, Specification developer | 4 | May 17, 2024 | 0 | 9 | 0 | api.fda.gov |
| Perimed AB | JARFALLA Stockholm, Sweden | Complaint file establishment, Manufacturer | 2 | October 22, 2013 | 0 | 0 | 0 | api.fda.gov |
| Radiometer Medical Aps | BROENSHOEJ Hovedstaden, Denmark | Complaint file establishment, Manufacturer | 2 | February 5, 2010 | 0 | 1 | 0 | api.fda.gov |
| Philips Medizin Systeme Boeblingen GmbH | BOEBLINGEN Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer, Specification developer | 1 | September 30, 2011 | 0 | 0 | 0 | api.fda.gov |
| Sechrist Industries, Inc. | Anaheim, CA, United States | Manufacturer | 1 | April 10, 1991 | 0 | 0 | 0 | api.fda.gov |
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Boyd Corporation GmbH | Syke Lower Saxony, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pulsion Medical Systems Se | Aschheim, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Murrysville, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Export, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Radiometer Basel AG | BASEL Basel-Stadt, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Radiometer Solutions Sp. z o.o. | Stargard Zachodniopomorskie, Poland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Radiometer Sp. z o.o | Stargard Zachodniopomorskie, Poland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated May 17, 2024. 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.