# LGC Clinical Diagnostics, Inc. (manufacturer, Milford, MA): 2 new FDA device listings, incl. equipment, laboratory, general purpose, labeled or promoted for a spec

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | LGC Clinical Diagnostics, Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Milford, MA, US |
| New listings | 2 |
| Devices | Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use; Urinalysis Controls (Assayed And Unassayed) |
| Product codes | LXG, JJW |
| Device classes | Class I |
| Medical specialties | Clinical Chemistry |
| Brand names | KOVA™ Stain Human Urinalysis Reagent (var.); KOVA™ Stain Human Urinalysis Reagent; LQ CNTRL SIEMENS DIPTUBE (6 x 15mL) Com; KOVA LQT SIEMENS W MICRO (2 x 120mL) Com, product code: 11561696; KOVA LQT SIEMENS NONMICR (2 x 120mL) Com, product code: 11561695; KOVA LiquaTrol II Normal w/hCG, microsc, product code: 87122; KOVA-poc (10 x 5mL), product code: 88105; LIQUATROL ABNORMAL 2X120ML, product code: 87176 |
| First new listing | 2026-08-24 |
| Latest new listing | 2026-09-03 |
| FDA registration number | 3007088335 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- 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: 2026-11-04T21:52:36.524Z.
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.