LGC Clinical Diagnostics, Inc. (manufacturer, Cumberland Foreside, ME): 2 new FDA device listings, incl. urinalysis controls (assayed and unassayed)

LGC Clinical Diagnostics, Inc. (Cumberland Foreside, Maine): 2 new FDA device listings, incl. urinalysis controls (assayed and unassayed). Its amount of 2 is above the median of 1 (69th percentile). Dated 63 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-10-28, 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: 2 · 69th percentile of 2,570 DeviceEstablishmentPulse records · 2.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 3 related ME DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentLGC Clinical Diagnostics, Inc.
RoleManufacturer
Establishment typesManufacture Medical Device
LocationCumberland Foreside, ME, US
New listings2
DevicesUrinalysis Controls (Assayed And Unassayed); Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
Product codesJJW, LXG
Device classesClass I
Medical specialtiesClinical Chemistry
Brand namesKOVA LiquaTrol II Normal w/hCG, microsc, product code: 87122; KOVA LQT SIEMENS W MICRO (2 x 120mL) Com, product code: 11561696; Level II Normal w/ hCG and Microscopics, product code: 87123; KOVA LiquaTrol McKesson 4 x 25mL Dropper, product code: 89116; LQ CNTRL SIEMENS DIPTUBE (6 x 15mL) Com; LQ CNTRL MCK (10X5ML), product code: 89119; KOVA POC Diptube w/ Microscopics 6x15mL, product code: 88115; LQ CNTRL CRDNL (6X15ML), product code: 89209
First new listing2026-08-24
Latest new listing2026-09-03
FDA registration number1226774
Registration expires2026-12-31
amount percentile69th of 2,570 (median 1, 2.0x median)
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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: 2026-10-28
  • 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, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: LGC Clinical Diagnostics, Inc. and 4 Maine peers

  • Maine DeviceEstablishmentPulse records like this one: 4
  • LGC Clinical Diagnostics, Inc.'s amount: 69th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Maine peer: $800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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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 Cumberland Foreside, Maine?

LGC Clinical Diagnostics, Inc. (Cumberland Foreside, ME), a manufacturer, added 2 FDA device listings between 2026-08-24 and 2026-09-03.

How does LGC Clinical Diagnostics, Inc. compare to other Maine DeviceEstablishmentPulse records?

Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 63 days old; check the official source for later updates before acting.

LGC Clinical Diagnostics, Inc. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
LGC Clinical Diagnostics, Inc.Cumberland Foreside, ME269th2026-09-03
Beacon Biosignals, Inc.Boston, MA377th2026-10-16
Endovascular Engineering, Inc.Menlo Park, CA377th2026-10-14
INNO Holdings Inc.Millcreek, UT377th2026-10-05

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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.

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