FdaApprovalPulse: records in California
110 fdaApprovalPulse: records in California are listed from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-05-01 to 2026-10-22; the most frequent is ABBOTT MEDICAL with 20. Data last updated 2026-11-03; 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
110 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-05-01 to 2026-10-22. Most frequent: ABBOTT MEDICAL (20). Each record links to a full report and the official source.
Last updated 2026-11-03. Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
Get new FdaApprovalPulse records by email (free, weekly)
We email one confirmation link now; the weekly digest starts only after you confirm. One-click unsubscribe in every email.
Double opt-in: nothing is sent until you click the confirmation link. One-click unsubscribe.
- ABBOTT MEDICAL (20)
- Edwards Lifesciences, LLC (13)
- Boston Scientific Corp (8)
- Guardant Health, Inc. (7)
- Allergan (4)
How do I get new fdaApprovalPulse: records in California by email?
Search, filter and export these records, or get alerts when new ones appear.
What are the top fdaApprovalPulse: records in California right now?
| Record | Product | Approval | Decided |
|---|---|---|---|
| Edwards Lifesciences, LLC | Edwards SAPIEN 3 Ultra RESILIA Transcatheter Heart Valve | PMA supplement (device change) | 2026-10-22 |
| Edwards Lifesciences, LLC | INSPIRIS RESILIA Aortic Valve; MITRIS RESILIA Mitral Valve | PMA supplement (device change) | 2026-10-22 |
| Edwards Lifesciences, LLC | PASCAL Precision Transcatheter Valve Repair System | PMA supplement (device change) | 2026-10-22 |
| ABBOTT MEDICAL | AVEIR VR Real-World Evidence Study | PMA supplement (device change) | 2026-10-21 |
| Edwards Lifesciences, LLC | EVOQUE Tricuspid Valve Replacement System | PMA supplement (device change) | 2026-10-21 |
| Edwards Lifesciences, LLC | PASCAL Precision Transcatheter Valve Repair System | PMA supplement (device change) | 2026-10-20 |
| Edwards Lifesciences, LLC | Edwards EVOQUE Tricuspid Valve Replacement System | PMA supplement (device change) | 2026-10-19 |
| Balt USA, LLC | SQUID Liquid Embolic Agent (LEA) | PMA supplement (device change) | 2026-10-16 |
| Boston Scientific Corp | Vercise DBS Systems | PMA supplement (device change) | 2026-10-15 |
| Ev3 Neurovascular | Onyx Liquid Embolic System (Onyx LES) | PMA supplement (device change) | 2026-10-14 |
| Edwards Lifesciences, LLC | Autus Size-Adjustable Valve | PMA original approval (new class III device) | 2026-10-01 |
| MedAlliance, LLC | SELUTION SLR 014 PTCA Drug-Eluting Balloon | PMA original approval (new class III device) | 2026-09-18 |
| Spineart USA, Inc. | BAGUERA®C Cervical Disc Prosthesis | PMA original approval (new class III device) | 2026-08-10 |
| Freenome, LLC | SimpleScreen CRC | PMA original approval (new class III device) | 2026-07-24 |
| Guardant Health, Inc. | Guardant360® Liquid CDx | PMA original approval (new class III device) | 2026-05-19 |
| Motiva USA, LLC | 🔒 Unlock all 110 records → | ||
| Allergan | 🔒 Unlock all 110 records → | ||
| Medtronic Minimed, Inc. | 🔒 Unlock all 110 records → | ||
Browse 35 more matching record reports
- Motiva USA, LLC
- Allergan
- Medtronic Minimed, Inc.
- Motiva USA, LLC
- ABBOTT MEDICAL
- Edwards Lifesciences, LLC
- Spineart USA, Inc.
- Boston Scientific Corp
- Boston Scientific Corp
- Guardant Health, Inc.
- Edwards Lifesciences, LLC
- Agilent Technologies, Inc.
- Boston Scientific Corp
- Pulmonx Corporation
- Medtronic, Inc.
- Boston Scientific Corp
- Balt USA, LLC
- Guardant Health, Inc.
- Farapulse, Inc.
- Rxsight, Inc.
- Biosense Webster, Inc.
- ABBOTT MEDICAL
- Renata Medical, Inc.
- Abbott Vascular, Inc.
- Farapulse, Inc.
- Neuspera Medical, Inc.
- Nevro Corporation
- Illumina, Inc.
- Recor Medical, Inc.
- Allergan
- Allergan
- Irvine Biomedical, Inc.
- Guardant Health, Inc.
- Irvine Biomedical, Inc.
- Irvine Biomedical,Inc.(Ibi)
Which related categories and locations should I check?
Browse by approval type
Drug labeling or REMS supplement (1174) PMA supplement (device change) (367) Generic drug approval (ANDA) (194) Drug efficacy supplement (new indication or use) (76) Drug manufacturing (CMC) supplement (55) New drug application (NDA) (40) PMA original approval (new class III device) (24) Biologic license (BLA) (17) Other drug supplement (12)
Browse by sponsor state (devices)
Minnesota (61) Massachusetts (37) Oregon (20) Arizona (18) Texas (18) Illinois (9) Maryland (9) Tennessee (8) Pennsylvania (7) Florida (6) Washington (6) Missouri (5) Wisconsin (5) Colorado (4) Connecticut (4) Georgia (4) Indiana (4) New Jersey (4) New York (4) North Carolina (3) Ohio (3)
More California public-record feeds
Nursing Home Inspection Deficiencies by State & Severity in California EPA Brownfields Award Tracker in California Industrial Environmental Noncompliance Radar in California New Trucking Company Registrations in California Largest U.S. Greenhouse Gas Emitters by Company, Sector & State (EPA GHGRP) in California CMS HAC Reduction & Readmissions Penalties by Hospital in California Carrier Out-of-Service Alerts in California New FDA Medical Device Listings by Manufacturer, CMO & Sterilizer in California
Frequently asked questions
How many fdaApprovalPulse: records in California are listed?
110 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), last refreshed automatically. The most recent is dated 2026-10-22.
Can I get alerts for California?
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