Insitu Technologies, Inc. (repackager or relabeler, Saint Paul, MN): 1 new FDA device listing, incl. catheters, transluminal coronary angioplasty, percutaneous
Insitu Technologies, Inc. (Saint Paul, Minnesota): 1 new FDA device listing, incl. catheters, transluminal coronary angioplasty, percutaneous. Its amount of 1 is above the median of 1 (50th percentile). Dated 21 days ago, it is in the active follow-up window. Score 60/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 1 · 50th percentile of 2,570 DeviceEstablishmentPulse records · 1.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 42 related MN DeviceEstablishmentPulse records and the 5-column CSV export.
| 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 |
| amount percentile | 50th of 2,570 (median 1, 1.0x median) |
| Peer records CSV (43 MN records) | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-10-14
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (MN first): Boston Scientific Corporation (manufacturer, Saint Paul, MN) · EPIC MedTec OEM Catheter & Wire LLC (contract manufacturer, · Isomedix Operations, Inc. (contract sterilizer, Minneapolis, · Rms Co. (contract manufacturer, Minneapolis, MN) · Boston Scientific Corporation (specification developer, Mapl · Browse all by state and category →
LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Insitu Technologies, Inc. and 43 Minnesota peers
- Minnesota DeviceEstablishmentPulse records like this one: 43
- Insitu Technologies, Inc.'s amount: 50th percentile of 2,570 records
- Timing: Medium: dated in the last 30 days
- Estimated pipeline if you contact every Minnesota peer: $8,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
60 / 100 Score
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Insitu Technologies, Inc. in Saint Paul, Minnesota?
Insitu Technologies, Inc. (Saint Paul, MN), a repackager or relabeler, added 1 FDA device listing on 2026-10-14.
How does Insitu Technologies, Inc. compare to other Minnesota DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,570 records; the median is 1. It is 21 days old, still within a typical 45-day follow-up window.
Insitu Technologies, Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Insitu Technologies, Inc. | Saint Paul, MN | 1 | 50th | 2026-10-14 |
| Nam Ha Viet Nam Trading Company Limited | Hanoi Ha Noi, VN | 3 | 77th | 2026-09-24 |
| Tpc Advanced Technology, Inc. | City Industry, CA | 4 | 83rd | 2026-09-28 |
| VIVE Health LLC | Naples, FL | 10 | 93rd | 2026-10-14 |
Related records
DeviceEstablishmentPulse: Repackager or relabeler DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Minnesota
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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.