Data / Medical devices / United States / Kenlor Industries, Inc.
Kenlor Industries, Inc.: FDA-registered device maker in Santa Ana, CA, United States, 2 510(k) clearances
Kenlor Industries, Inc. is registered with the FDA (registration 2027370) in Santa Ana, CA, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 3, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2027370
- Address
- 1560 East Edinger Ave. Suite A-1, Santa Ana, CA, United States, 92705
- Owner or operator
- KENLOR INDUSTRIES, INC. (2027370)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- July 1, 2016
- Registered through
- 2026
- Brand names listed
- H Pylori, Liquid Urine Control
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Helicobacter Pylori | LYR | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Urinalysis Controls (Assayed And Unassayed) | JJW | 1 | Contract manufacturer, Manufacturer | 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 |
|---|---|---|---|---|---|---|
| March 3, 1997 | K964014 | KENLOR H. PYLORI CONTROL SERUM | LYR | Substantially Equivalent | Kenlor Industries, Inc. | accessdata.fda.gov |
| March 9, 1989 | K890577 | KENLOR LIQUID URINE CONTROL | JJW | Substantially Equivalent | Kenlor Industries, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 3, 1997. 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.