# Icp, Inc. (specification developer, Green Bay, WI): 5 new FDA device listings, incl. band, elastic, orthodontic

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Icp, Inc. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility |
| Location | Green Bay, WI, US |
| New listings | 5 |
| Devices | Band, Elastic, Orthodontic; Bur, Dental; Mouthpiece, Saliva Ejector; Indicator, Physical/Chemical Sterilization Process; Wrap, Sterilization |
| Product codes | ECI, EJL, DYN, JOJ, FRG |
| Device classes | Class I, Class II |
| Medical specialties | Dental, General Hospital |
| First new listing | 2026-05-21 |
| Latest new listing | 2026-05-21 |
| FDA registration number | 2132509 |
| Registration expires | 2026-12-31 |

## 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.

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.