Data / Medical devices / United States / Caplugs, Inc.
Caplugs, Inc.: FDA-registered device maker in Rancho Dominguez, CA, United States, 1 510(k) clearance
Caplugs, Inc. is registered with the FDA (registration 2016673) in Rancho Dominguez, CA, United States. It lists 12 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 28, 1983. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2016673
- Address
- 18704 S Ferris Pl, Rancho Dominguez, CA, United States, 90220
- Owner or operator
- Caplugs, Inc. (10050609)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- December 8, 2015
- Registered through
- 2027
- Brand names listed
- 95 pin inoculator - sterile, Centrifuge Tubes, Collection/Transport Containers - sterile, Collection/transport Containers - non sterile, Disposable Columns, Disposables for use with Abbott TDx, Embedding rings/processing & Embedding cassettes, FPC Fecal Parasite Concentrators and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adsorbents, Ion-Exchange | DKO | 1 | Manufacturer | accessdata.fda.gov |
| Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use | JJC | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen Mailer And Storage, Sterile | KDT | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen, Non-Sterile | NNI | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen, Sterile | FMH | 1 | Manufacturer | accessdata.fda.gov |
| Device, General Purpose, Microbiology, Diagnostic | LIB | 1 | Manufacturer | accessdata.fda.gov |
| Device, Microtiter Diluting/Dispensing | JTC | 1 | Manufacturer | accessdata.fda.gov |
| Device, Parasite Concentration | LKS | 1 | Manufacturer | accessdata.fda.gov |
| Filters, Cell Collection, Tissue Processing | KET | 1 | Manufacturer | accessdata.fda.gov |
| Hydrazone Deriv. Of Alpha-Ketogluterate (Colorimetry), Isocitric Dehydrogen | JKH | 1 | Manufacturer | accessdata.fda.gov |
| Slides, Microscope | KEW | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Station, Pipetting And Diluting, For Clinical Use | JQW | 1 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 28, 1983 | K833469 | FPC FECAL PARASITE CONCENTRATOR | LKS | Substantially Equivalent | Evergreen Scientific, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Container, Specimen, Non-Sterile
- All makers of Station, Pipetting And Diluting, For Clinical Use
- All makers of Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use
- All makers of Container, Specimen, Sterile
- All makers of Device, Microtiter Diluting/Dispensing
Updated November 28, 1983. 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.