# Forsure Medical Products LLC. (repackager or relabeler, Doral, FL): 10 new FDA device listings, incl. tube, tracheostomy (w/wo connector)

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Forsure Medical Products LLC. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Doral, FL, US |
| New listings | 10 |
| Devices | Tube, Tracheostomy (W/Wo Connector); Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days; Device, Incontinence, Urosheath Type, Non-Sterile; Bedding, Disposable, Medical; Tubes, Gastrointestinal (And Accessories); Catheter, Retention Type, Balloon; Instrument, Surgical, Disposable; Needle, Hypodermic, Single Lumen; Syringe, Piston; Stapler, Skin |
| Product codes | BTO, FOZ, NNX, KME, KNT, EZL, KDC, FMI, FMF, QQS |
| Device classes | Class I, Class II |
| Medical specialties | Anesthesiology, General Hospital, Gastroenterology, Urology, General, Plastic Surgery |
| Brand names | Forsure Tracheostomy Tube; Forsure IV Catheter; Forsure Male External Catheter; Forsure Disposable Underpad; Forsure Stomach Tube; Forsure Silicone and Latex Foley Catheters; Forsure Skin Staple Remover; Forsure Hypodermic Needle |
| First new listing | 2026-05-14 |
| Latest new listing | 2026-06-16 |
| FDA registration number | 3005609751 |
| Registration expires | 2026-12-31 |

## Why this score
- 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.