Boulder Biomed LLC (contract sterilizer, Boulder, CO): 2 new FDA device listings, incl. clamp, vascular
Boulder Biomed LLC (Boulder, Colorado): 2 new FDA device listings, incl. clamp, vascular. Its amount of 2 is above the median of 1 (69th percentile). Dated 44 days ago, it serves as a historical benchmark. Score 75/100. 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: 2 · 69th percentile of 2,570 DeviceEstablishmentPulse records · 2.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 32 related CO DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Boulder Biomed LLC |
| Owner / operator | Boulder BioMed dba Boulder iQ |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer) |
| Location | Boulder, CO, US |
| New listings | 2 |
| Devices | Clamp, Vascular; Fastener, Fixation, Nondegradable, Soft Tissue |
| Product codes | DXC, MBI |
| Device classes | Class II |
| Medical specialties | Cardiovascular, Orthopedic |
| Brand names | Vascular Clamp; RapidFix All-Suture Dual Anchor |
| First new listing | 2026-07-10 |
| Latest new listing | 2026-09-22 |
| FDA registration number | 3015151147 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,570 (median 1, 2.0x median) |
| Peer records CSV (33 CO records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 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: 2026-09-22
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (CO first): Simple Style Inc (specification developer, Brighton, CO) · Paragon 28 (manufacturer, Englewood, CO) · Terumo BCT STERILIZATION SERVICES, Inc. (contract sterilizer · Altivera Medical, Inc. (repackager or relabeler, Englewood, · Covidien (specification developer, Lafayette, CO) · 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: Boulder Biomed LLC and 33 Colorado peers
- Colorado DeviceEstablishmentPulse records like this one: 33
- Boulder Biomed LLC's amount: 69th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Colorado peer: $6,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
75 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Boulder Biomed LLC in Boulder, Colorado?
Boulder Biomed LLC (Boulder, CO), a contract sterilizer, added 2 FDA device listings between 2026-07-10 and 2026-09-22.
How does Boulder Biomed LLC compare to other Colorado DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 44 days old, still within a typical 45-day follow-up window. Its Score of 75/100 puts it among the stronger signals in this feed.
Boulder Biomed LLC vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Boulder Biomed LLC | Boulder, CO | 2 | 69th | 2026-09-22 |
| Isomedix Operations Inc. | Chester, NY | 3 | 77th | 2026-09-28 |
| Isomedix Operations, Inc | Ontario, CA | 7 | 90th | 2026-10-15 |
| Isomedix Operations, Inc. | Libertyville, IL | 7 | 90th | 2026-10-15 |
Related records
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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.