# Insitu Technologies, Inc. (repackager or relabeler, Saint Paul, MN): 1 new FDA device listing, incl. catheters, transluminal coronary angioplasty, percutaneous

**Score:** 60/100

| Field | Value |
|---|---|
| Establishment | Insitu Technologies, Inc. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Saint Paul, MN, US |
| New listings | 1 |
| Devices | Catheters, Transluminal Coronary Angioplasty, Percutaneous |
| Product codes | LOX |
| Device classes | Class II |
| Medical specialties | Cardiovascular |
| Brand names | AaRiss DCB |
| First new listing | 2026-10-14 |
| Latest new listing | 2026-10-14 |
| FDA registration number | 2134244 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- 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: 2026-10-28T20:51:27.468Z.
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.