# Yizur Ltd (repackager or relabeler, Hong Kong, HK): 101 new FDA device listings, incl. applicator, absorbent tipped, non-sterile

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Yizur Ltd |
| Role | Repackager or relabeler |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device; Repack or Relabel Medical Device |
| Location | Hong Kong, HK |
| New listings | 101 |
| Devices | Applicator, Absorbent Tipped, Non-Sterile; Aligner, Bracket, Orthodontic; Tube Impression And Matrix; Wrap, Sterilization; Floss, Dental; Dispenser, Liquid Medication; Scaler, Periodontic; Instrument, Hand, Calculus Removal; Accessory, Surgical Apparel; Powder, Porcelain |
| Product codes | KXF, ECQ, KCQ, FRG, JES, KYX, EMN, ELA, LYU, EIH, EIY, EKR, JOJ, EHL, KHR |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | General Hospital, Dental, General, Plastic Surgery, Orthopedic, Ear, Nose, Throat |
| Brand names | Applicator, Absorbent Tipped, Non-Sterile; Tips; Pouch; Retraction Cord; DISPENSER, LIQUID MEDICATION; Scaler; INSTRUMENT, HAND, CALCULUS REMOVAL; Face Shield |
| First new listing | 2026-05-06 |
| Latest new listing | 2026-10-07 |
| FDA registration number | 3045855232 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- Listed in the last 45 days.

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.