Cordis US Corporation: PMA supplement approved for PRECISE PRO RX Nitinol Stent System
Cordis US Corporation (Miami Lakes, Florida): PMA supplement approved for PRECISE PRO RX Nitinol Stent System. Dated 152 days ago, it serves as a historical benchmark. Score 30/100. As of 2026-11-04, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
Free preview: all 8 published fields of this record are shown below. Locked: 5 related FL FdaApprovalPulse records and the 4-column CSV export.
| Field | Value |
|---|---|
| Sponsor | Cordis US Corporation |
| Product | PRECISE PRO RX Nitinol Stent System |
| Generic / ingredient | Stent, carotid |
| Approval | PMA supplement (device change) |
| Application | P030047 S055 |
| Decided | 2026-06-05 |
| Panel / class | Cardiovascular |
| Sponsor location | Miami Lakes, FL |
| Peer records CSV (6 FL records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Sponsor · Product · Approval · Decided · official source URL
- Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
- Record date: 2026-06-05
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
Top FdaApprovalPulse records (FL first): Cerenovus, Inc. · Lenstec, Inc. · Biomet Microfixation, Inc. · Cordis US Corporation · Cordis US Corporation · Browse all by state and category →
LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 06:06:18 GMT
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Peer benchmark and outreach value: Cordis US Corporation and 6 Florida peers
- Florida FdaApprovalPulse records like this one: 6
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Florida peer: $1,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
30 / 100 Score
What is the FdaApprovalPulse record for Cordis US Corporation in Miami Lakes, Florida?
The FDA approved PRECISE PRO RX Nitinol Stent System (P030047 S055) for Cordis US Corporation on 2026-06-05: PMA supplement (device change).
How does Cordis US Corporation compare to other Florida FdaApprovalPulse records?
It is 152 days old; check the official source for later updates before acting. Its Score of 30/100 is modest; treat it as background rather than a priority.
Cordis US Corporation vs. top 2 peers
| Organization | Location | Record date |
|---|---|---|
| Cordis US Corporation | Miami Lakes, FL | 2026-06-05 |
| Cerenovus, Inc. | Miami, FL | 2026-10-23 |
| Lenstec, Inc. | St. Petersburg, FL | 2026-10-23 |
Related records
FdaApprovalPulse: PMA supplement (device change) FdaApprovalPulse: records in Florida
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From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.