# North American Rescue, LLC. (manufacturer, Greer, SC): 5 new FDA device listings, incl. kit, surgical instrument, disposable

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | North American Rescue, LLC. |
| Role | Manufacturer |
| Establishment types | Repack or Relabel Medical Device; Manufacture Medical Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Greer, SC, US |
| New listings | 5 |
| Devices | Kit, Surgical Instrument, Disposable; Burn Kit Without Drug; Device, Intravascular Catheter Securement; Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear); Airway Suction Kit |
| Product codes | KDD, OJJ, KMK, HOY, OFO |
| Device classes | Class I |
| Medical specialties | General, Plastic Surgery, General Hospital, Ophthalmic, Anesthesiology |
| Brand names | NAR Surgical Disposal Kit; NAR Surgical Suture Kit; Burntec Kit; Raptor; Polycarbonate Eye Shield; Fox Eye Shield; King LTS-D Airway Kit; King Airway Kit |
| First new listing | 2026-06-15 |
| Latest new listing | 2026-07-17 |
| FDA registration number | 3005034064 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- 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: 2026-11-04T21:52:36.524Z.
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.