Kenlor Industries, Inc.
FDA Regulatory Profile
Kenlor Industries, Inc. has 0 FDA recalls, 2 inspections, 9 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Sep 21, 2020 · VAI
- Latest 510(k)
- Mar 3, 1997
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 0 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 9 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 2 | Nov 9, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent FDA Inspections
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 2027370 | Santa Ana, CA | 2 | Sep 21, 2020 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K964014 | KENLOR H. PYLORI CONTROL SERUM | Mar 3, 1997 |
| K952840 | KENLOR LIQUID TOTAL URINE CONTROL | Jul 19, 1995 |
| K950326 | KENLOR HUMAN SPINAL FLUID CONTROL | Mar 20, 1995 |
| K903338 | KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL | Sep 7, 1990 |
| K896440 | KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT | Feb 16, 1990 |
| K890618 | COOMASSIE BLUE TOTAL PROTEIN ASSAY KIT | May 22, 1989 |
| K890573 | KENLOR TOTAL IRON, UIBC/TIBC ASSAY KIT | Mar 24, 1989 |
| K890576 | KENLOR HUMAN SPINAL FLUID CONTROL LIQUID | Mar 9, 1989 |
| K890577 | KENLOR LIQUID URINE CONTROL | Mar 9, 1989 |