FdaApprovalPulse: records in Minnesota
61 fdaApprovalPulse: records in Minnesota are listed from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-05-01 to 2026-10-21; the most frequent is Medtronic, Inc. with 15. Data last updated 2026-11-04; each record links to its official source and a full report.
Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
Includes: Sponsor, Product, Approval, Decided, official source URL and score · Card, Apple Pay, Google Pay or Link via Stripe
61 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-05-01 to 2026-10-21. Most frequent: Medtronic, Inc. (15). Each record links to a full report and the official source.
Last updated 2026-11-04. Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
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- Medtronic, Inc. (15)
- ABBOTT MEDICAL (13)
- Boston Scientific Corp (6)
- Boston Scientific Corporation (5)
- DiaSorin, Inc. (4)
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What are the top fdaApprovalPulse: records in Minnesota right now?
| Record | Product | Approval | Decided |
|---|---|---|---|
| Boston Scientific Corp | ROTAPRO Rotational Atherectomy Systems | PMA supplement (device change) | 2026-10-21 |
| ABBOTT MEDICAL | Volt PFA System | PMA supplement (device change) | 2026-10-15 |
| DiaSorin, Inc. | LIAISON Biotrin Parvovirus B19 IgM Plus, LIAISON Biotrin Control Parvovirus B19 IgM Plus | PMA original approval (new class III device) | 2026-05-07 |
| Medtronic, Inc. | Sphere-9 Catheter and Affera Ablation System | PMA supplement (device change) | 2026-10-06 |
| Medtronic, Inc. | Activa Deep Brain Stimulation Therapy System, Percept PC BrainSense | PMA supplement (device change) | 2026-10-06 |
| Medtronic, Inc. | Sphere-9 Catheter and Affera Ablation System | PMA supplement (device change) | 2026-10-02 |
| Medtronic Cryocath, LP | STOP Persistent AF | PMA supplement (device change) | 2026-09-25 |
| Medtronic | HeartWare® HVAD System | PMA supplement (device change) | 2026-09-23 |
| ABBOTT MEDICAL | TactiFlex Ablation Catheter, Sensor Enabled | PMA supplement (device change) | 2026-09-22 |
| ABBOTT MEDICAL | TactiFlex Duo Ablation Catheter, Sensor Enabled (A-TFDM-D, A-TFDM-F, A-TFDM-J, A-TFDM-DD, A-TFDM-DF, A-TFDM-FF, A-TFDM | PMA supplement (device change) | 2026-09-04 |
| ABBOTT MEDICAL | Amplatzer Amulet Left Atrial Appendage Occluder | PMA supplement (device change) | 2026-08-28 |
| Inspire Medical Systems | Model 4063 Inspire Stimulation Lead | PMA supplement (device change) | 2026-08-28 |
| Inspire Medical Systems | INSPIRE II UPPER AIRWAY STIMULATOR | PMA supplement (device change) | 2026-08-28 |
| DiaSorin, Inc. | LIAISON QuantiFERON-TB Gold Plus; LIAISON XL Control QuantiFERON-TB Gold Plus; LIAISON QuantiFERON-TB Gold Plus II; LIAI | PMA supplement (device change) | 2026-08-27 |
| DiaSorin, Inc. | LIAISON QuantiFERON-TB Gold III; LIAISON Control QuantiFERON-TB Gold III; LIAISON QuantiFERON-TB Gold Plus II; LIAISON C | PMA supplement (device change) | 2026-08-27 |
| Boston Scientific Corp | 🔒 Unlock all 61 records → | ||
| DiaSorin, Inc. | 🔒 Unlock all 61 records → | ||
| St Jude Medical | 🔒 Unlock all 61 records → | ||
Browse 35 more matching record reports
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Drug labeling or REMS supplement (1180) PMA supplement (device change) (367) Generic drug approval (ANDA) (196) Drug efficacy supplement (new indication or use) (77) Drug manufacturing (CMC) supplement (55) New drug application (NDA) (41) PMA original approval (new class III device) (24) Biologic license (BLA) (17) Other drug supplement (12)
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Frequently asked questions
How many fdaApprovalPulse: records in Minnesota are listed?
61 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), last refreshed automatically. The most recent is dated 2026-10-21.
Can I get alerts for Minnesota?
Yes. FdaApprovalPulse can email you new records matching this filter; plans are listed on the FdaApprovalPulse page.
Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration). Informational only. RSS feed of new records