# Skyward Medical Devices LLC (repackager or relabeler, Eastvale, CA): 28 new FDA device listings, incl. shield, protective, personnel

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Skyward Medical Devices LLC |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Eastvale, CA, US |
| New listings | 28 |
| Devices | Shield, Protective, Personnel; Vibrator For Therapeutic Use, Genital; Catheter, Eustachian, General & Plastic Surgery; Sling, Arm; Portable Liquid Oxygen Unit Stand; Crutch; Orthosis, Thoracic; Apparatus, Suction, Operating-Room, Wall Vacuum Powered; Shoe, Cast; Support, Arm |
| Product codes | KPY, KXQ, GBY, ILI, PCM, IPR, IPT, GCX, IPG, IOY, FQM, OEA, KYS, HOY, PHW |
| Device classes | Class I, Class II |
| Medical specialties | Radiology, Obstetrics/Gynecology, General, Plastic Surgery, Physical Medicine, General Hospital, Ophthalmic, Ear, Nose, Throat, Anesthesiology, Dental |
| Brand names | Face Shield; Probe for Pelvic Floor Trainer, Kegel Exerciser Probe for Strengthen Pelvic Floor Muscle; Eustachian Tube Unblocker Ear Pressure Relief Device; Arm Sling; portable oxygen unit TRB-140; Crutch; Hyperextension Brace;Prefabricated Hyperextension Orthosis,TRB-401; Portable Suction Machine for Home,Electric Suction Machine |
| First new listing | 2026-08-03 |
| Latest new listing | 2026-08-03 |
| FDA registration number | 3043009869 |
| 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.