# HyperFlex Medical Inc (specification developer, Richmond, UT): 2 new FDA device listings, incl. instrument, compression

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | HyperFlex Medical Inc |
| Owner / operator | HyperFlex Medical Inc. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Richmond, UT, US |
| New listings | 2 |
| Devices | Instrument, Compression; Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment |
| Product codes | HWN, HWE |
| Device classes | Class I |
| Medical specialties | Orthopedic, General, Plastic Surgery |
| First new listing | 2026-09-17 |
| Latest new listing | 2026-09-17 |
| FDA registration number | 3038503572 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- 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.