Lightning X Products, Inc (manufacturer, Charlotte, NC): 32 new FDA device listings, incl. airway, oropharyngeal, anesthesiology

Lightning X Products, Inc (Charlotte, North Carolina): 32 new FDA device listings, incl. airway, oropharyngeal, anesthesiology. Its amount of 32 is top-decile (98th percentile of 2,570 records). Dated 54 days ago, it serves as a historical benchmark. Score 85/100. 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: 32 · 98th percentile of 2,570 DeviceEstablishmentPulse records · 32.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 32 related NC DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentLightning X Products, Inc
RoleManufacturer
Establishment typesRepack or Relabel Medical Device; Manufacture Medical Device
LocationCharlotte, NC, US
New listings32
DevicesAirway, Oropharyngeal, Anesthesiology; Orthosis, Cervical; Forceps; Tape And Bandage, Adhesive; Pack, Hot Or Cold, Disposable; Stethoscope, Manual; Polymer Patient Examination Glove; Pad, Eye; Mask, Oxygen, Non-Rebreathing; Bedding, Disposable, Medical
Product codesCAE, IQK, HTD, KGX, IMD, LDE, LZA, HMP, KGB, KME, ILI, LKB, DXN, FZQ, SDV
Device classesClass I, Class II, Not classified, Unclassified
Medical specialtiesAnesthesiology, Physical Medicine, General, Plastic Surgery, General Hospital, Cardiovascular
Brand namesLightning X Berman Airway Kit; Lightning X Perfect Fit Adult Adjustable Extrication Cervical Collar; Lightning X Kelly Forceps; Lightning X Tweezer Forceps; Lightning X 2" Cloth Medical Tape; Lightning X 1" Cloth Medical Tape; Lightning X Instant Cold Pack; Lightning X Sprague Stethoscope
First new listing2026-08-30
Latest new listing2026-09-11
FDA registration number3012311599
Registration expires2027-12-31
amount percentile98th of 2,570 (median 1, 32.0x 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: 2026-09-11
  • 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: Lightning X Products, Inc and 33 North Carolina peers

  • North Carolina DeviceEstablishmentPulse records like this one: 33
  • Lightning X Products, Inc's amount: 98th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every North Carolina peer: $6,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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85 / 100 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.

What is the DeviceEstablishmentPulse record for Lightning X Products, Inc in Charlotte, North Carolina?

Lightning X Products, Inc (Charlotte, NC), a manufacturer, added 32 FDA device listings between 2026-08-30 and 2026-09-11.

How does Lightning X Products, Inc compare to other North Carolina DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 32 is 32.0x the median of 1 across 2,570 records. It is 54 days old; check the official source for later updates before acting. Its Score of 85/100 puts it among the stronger signals in this feed.

Lightning X Products, Inc vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Lightning X Products, IncCharlotte, NC3298th2026-09-11
Boston Scientific CorporationSaint Paul, MN2498th2026-10-16
Ge Parallel Design, Inc.Phoenix, AZ1997th2026-10-07
Surgentec LLCBoca Raton, FL1596th2026-10-16

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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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