# Victorch Meditek, Inc. (manufacturer, San Diego, CA): 15 new FDA device listings, incl. applicator, absorbent tipped, sterile

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Victorch Meditek, Inc. |
| Owner / operator | Victorch Meditek Inc |
| Role | Manufacturer |
| Establishment types | Manufacture Device in the United States for Export Only |
| Location | San Diego, CA, US |
| New listings | 15 |
| Devices | Applicator, Absorbent Tipped, Sterile; Antisera, Fluorescent, Chlamydia Spp.; Wrap, Sterilization; Device, Neurovascular Embolization; Antigen(Complexed),Prostate Specific,(Cpsa); Single (Specified) Analyte Controls (Assayed And Unassayed); Multi-Analyte Respiratory Virus Antigen Detection Test; Test, Luteinizing Hormone (Lh), Over The Counter; Control, Fecal Occult Blood; Scissors, Medical, Disposable |
| Product codes | KXG, LKI, FRG, HCG, NAF, JJX, SCA, NGE, OSL, JOK, LQP, LIP, DDG, LOJ, DJC |
| Device classes | Class I, Class II, Class III |
| Medical specialties | General Hospital, Microbiology, Neurology, Clinical Chemistry, Hematology, Immunology, Clinical Toxicology |
| Brand names | Nasopharyngeal Swab; Chlamydia Rapid Test; Hemostatic Patch Bag; HCG pregnancy Urine Rapid Test, HCG Midstream Rapid Test; PSA Rapid Test; CEA Rapid Test; Covid-19/Flu A/Alu B/RSV Rapid Test; LH Rapid test |
| First new listing | 2026-06-30 |
| Latest new listing | 2026-07-02 |
| FDA registration number | 2032364 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.