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

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Lightning X Products, Inc |
| Role | Manufacturer |
| Establishment types | Repack or Relabel Medical Device; Manufacture Medical Device |
| Location | Charlotte, NC, US |
| New listings | 32 |
| Devices | Airway, 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 codes | CAE, IQK, HTD, KGX, IMD, LDE, LZA, HMP, KGB, KME, ILI, LKB, DXN, FZQ, SDV |
| Device classes | Class I, Class II, Not classified, Unclassified |
| Medical specialties | Anesthesiology, Physical Medicine, General, Plastic Surgery, General Hospital, Cardiovascular |
| Brand names | Lightning 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 listing | 2026-08-30 |
| Latest new listing | 2026-09-11 |
| FDA registration number | 3012311599 |
| Registration expires | 2027-12-31 |

## Why this 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.

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: 2026-10-28T20:51:27.468Z.
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.