Aurora Gp Lab Inc (contract manufacturer, Goodyear, AZ): 6 new FDA device listings, incl. lens, contact, orthokeratology, overnight

Aurora Gp Lab Inc (Goodyear, Arizona): 6 new FDA device listings, incl. lens, contact, orthokeratology, overnight. Its amount of 6 is above the median of 1 (88th percentile). Dated 147 days ago, it serves as a historical benchmark. Score 80/100. 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: 6 · 88th percentile of 2,570 DeviceEstablishmentPulse records · 6.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 14 related AZ DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentAurora Gp Lab Inc
Owner / operatorAurora GP Lab Inc
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationGoodyear, AZ, US
New listings6
DevicesLens, Contact, Orthokeratology, Overnight; Lens, Contact (Other Material) - Daily; Lens, Contact (Orthokeratology)
Product codesNUU, HQD, MUW
Device classesClass II, Class III
Medical specialtiesOphthalmic
Brand namesSee Z (Tisifocon A); OrthCyl (tisilfocon A) Rigid Gas Permeable Contact Lens for Orthokeratology - Overnight Wear; See Z Tangent (tisilfocon A) Rigid Gas Permeable Contact Lens for Orthokeratology - Overnight Wear; See Z Tangent (Tisifocon A); OrthCyl X-Toric (tisilfocon A) Rigid Gas Permeable Contact Lens for Orthokeratology - Overnight Wear; See Z (tisilfocon A) Rigid Gas Permeable Contact Lens for Orthokeratology - Overnight Wear; Nuvea Sphere (Rofufocon E); Nuvea Scleral (Rofufocon D)
First new listing2026-05-05
Latest new listing2026-06-10
FDA registration number3045320731
Registration expires2026-12-31
amount percentile88th of 2,570 (median 1, 6.0x 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: 2026-06-10
  • 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: Aurora Gp Lab Inc and 15 Arizona peers

  • Arizona DeviceEstablishmentPulse records like this one: 15
  • Aurora Gp Lab Inc's amount: 88th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Arizona peer: $3,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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80 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for Aurora Gp Lab Inc in Goodyear, Arizona?

Aurora Gp Lab Inc (Goodyear, AZ), a contract manufacturer, added 6 FDA device listings between 2026-05-05 and 2026-06-10.

How does Aurora Gp Lab Inc compare to other Arizona DeviceEstablishmentPulse records?

Its amount of 6 sits in the upper half (88th percentile) of 2,570 records; the median is 1. It is 147 days old; check the official source for later updates before acting. Its Score of 80/100 puts it among the stronger signals in this feed.

Aurora Gp Lab Inc vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Aurora Gp Lab IncGoodyear, AZ688th2026-06-10
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16
Cook Medical LLCBloomington, IN483rd2026-10-13
Swiss-American CDMO,LLCCarrollton, TX483rd2026-10-12

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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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