Data / Medical devices / Strip, Temperature, Forehead, Liquid Crystal
Strip, Temperature, Forehead, Liquid Crystal (KPD): 18 FDA-registered makers in 5 countries
18 establishments in 5 countries are registered with the FDA to make Strip, Temperature, Forehead, Liquid Crystal (product code KPD, Class 2, 21 CFR 880.2200). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 21 510(k) clearances under this code, the latest on July 27, 1994, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- KPD
- Device class
- 2
- Regulation
- 880.2200
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| China | 9 |
| United States | 5 |
| Taiwan | 2 |
| Mexico | 1 |
| Thailand | 1 |
Makers of Strip, Temperature, Forehead, Liquid Crystal
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 |
|---|---|---|---|---|---|---|---|---|
| American Thermal Instruments, LLC | Dayton, OH, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Acute Ideas Co., Ltd. | Taipei, Taiwan | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chants (foshan) Technology Co.,ltd | Foshan Guangdong, China | Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Deroyal Industries, Inc. | Powell, TN, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dongguan E-Test Technology Co.,ltd | Dongguan Guangdong, China | Complaint file establishment, Foreign private label distributor, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dongyang City Yonoel Outdoor Products Co.,ltd | Dongyang Zhejiang, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fourstar Group Inc. | Taipei, Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Dexin Sports Industry Co.,ltd | Guangzhou Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| International Biomedical, Ltd. | Austin, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LCR Hallcrest, LLC. (IL) | Glenview, IL, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Tianbo First Aid Product Co., Ltd. | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Planet (anhui) Medical Products Co., Ltd | Chuzhou Anhui, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Productos Urologos De Mexico S.A. De C.V. | MEXICALI Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Puli Healthcare (thailand) Co., Ltd. | Bangkok Samut Prakan, Thailand | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Saferlife Products Co.,ltd. | Guangzhou Guangdong, China | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Joose Beauty Electronic Co.,ltd | Shen Zhen Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Pulikang Medical Device Co Ltd | Suzhou Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated July 27, 1994. 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.