LGC Clinical Diagnostics, Inc. (manufacturer, Gaithersburg, MD): 1 new FDA device listing, incl. urinalysis controls (assayed and unassayed)
LGC Clinical Diagnostics, Inc. (Gaithersburg, Maryland): 1 new FDA device listing, incl. urinalysis controls (assayed and unassayed). Its amount of 1 is above the median of 2 (50th percentile). Dated 64 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-11-04, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 1 · 50th percentile of 2,709 DeviceEstablishmentPulse records · 0.5x the median
Free preview: all 14 published fields of this record are shown below. Locked: 14 related MD DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | LGC Clinical Diagnostics, Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Gaithersburg, MD, US |
| New listings | 1 |
| Devices | Urinalysis Controls (Assayed And Unassayed) |
| Product codes | JJW |
| Device classes | Class I |
| Medical specialties | Clinical Chemistry |
| Brand names | 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; LQ CNTRL MCK (10X5ML), product code: 89119; LQ CNTRL MCKSN (4x120ML), product code: 89123 |
| First new listing | 2026-09-03 |
| Latest new listing | 2026-09-03 |
| FDA registration number | 3003610890 |
| Registration expires | 2026-12-31 |
| amount percentile | 50th of 2,709 (median 2, 0.5x median) |
| Peer records CSV (15 MD records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-09-03
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: LGC Clinical Diagnostics, Inc. and 15 Maryland peers
- Maryland DeviceEstablishmentPulse records like this one: 15
- LGC Clinical Diagnostics, Inc.'s amount: 50th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Maryland peer: $3,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
55 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for LGC Clinical Diagnostics, Inc. in Gaithersburg, Maryland?
LGC Clinical Diagnostics, Inc. (Gaithersburg, MD), a manufacturer, added 1 FDA device listing on 2026-09-03.
How does LGC Clinical Diagnostics, Inc. compare to other Maryland DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,709 records; the median is 2. It is 64 days old; check the official source for later updates before acting.
LGC Clinical Diagnostics, Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| LGC Clinical Diagnostics, Inc. | Gaithersburg, MD | 1 | 50th | 2026-09-03 |
| Applied Medical Resources Corp. | Rsm, CA | 3 | 77th | 2026-10-23 |
| Tornier, Inc. | Bloomington, MN | 3 | 77th | 2026-10-21 |
| Treace Medical Concepts, Inc. | Ponte Vedra, FL | 3 | 77th | 2026-10-20 |
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DeviceEstablishmentPulse: Manufacturer DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Maryland
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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.