# Inter-Med, Inc. (manufacturer, Racine, WI): 5 new FDA device listings, incl. cord, retraction

**Score:** 95/100

| Field | Value |
|---|---|
| Establishment | Inter-Med, Inc. |
| Role | Manufacturer |
| Establishment types | Repack or Relabel Medical Device; Manufacture Medical Device |
| Location | Racine, WI, US |
| New listings | 5 |
| Devices | Cord, Retraction; Agent, Tooth Bonding, Resin; Oral Wound Dressing; Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic; Cement, Dental |
| Product codes | MVL, KLE, OLR, MGQ, EMA |
| Device classes | Class II, Unclassified |
| Medical specialties | Dental |
| Brand names | Synvaza; REGEN Bioactive Cement |
| First new listing | 2026-05-19 |
| Latest new listing | 2026-10-22 |
| FDA registration number | 2133714 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
- 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: 2026-11-04T21:52:36.524Z.
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.