Data / Medical devices / Flowmeter, Nonback-Pressure Compensated, Bourdon Gauge
Flowmeter, Nonback-Pressure Compensated, Bourdon Gauge (CCN): 10 FDA-registered makers in 6 countries
10 establishments in 6 countries are registered with the FDA to make Flowmeter, Nonback-Pressure Compensated, Bourdon Gauge (product code CCN, Class 1, 21 CFR 868.2300). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 9 510(k) clearances under this code, the latest on November 17, 1993, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.
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- Product code
- CCN
- Device class
- 1
- Regulation
- 868.2300
- Medical specialty
- Anesthesiology
Makers by country
| Country | Makers |
|---|---|
| China | 3 |
| Taiwan | 2 |
| United States | 2 |
| Switzerland | 1 |
| Spain | 1 |
| Canada | 1 |
Makers of Flowmeter, Nonback-Pressure Compensated, Bourdon Gauge
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 |
|---|---|---|---|---|---|---|---|---|
| A Power Inst., Inc. | Taichung City, Taiwan | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Acare Technology Co., Ltd. | New Taipei City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Allied Medical LLC | Earth City, MO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Controls Corporation Of America | Virginia Beach, VA, United States | Contract manufacturer, Manufacturer, Manufacturer for export, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danyang Xinya Valve Co., Ltd. | Danyang Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gentec (shanghai) Corporation | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gloor Ltd. | Burgdorf Bern, Switzerland | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hersill, S.L. | MOSTOLES (MADRID) Madrid(Province), Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Mcare Medical Co.,ltd. | Danyang Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| O-Two Medical Technologies, Inc. | Brampton Ontario, Canada | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 17, 1993. 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.