FdaApprovalPulse: records in Florida
6 fdaApprovalPulse: records in Florida are listed from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-05-14 to 2026-10-23; the most frequent is Cordis US Corporation with 3. 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
6 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-05-14 to 2026-10-23. Most frequent: Cordis US Corporation (3). 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).
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- Cordis US Corporation (3)
- Lenstec, Inc. (1)
- Cerenovus, Inc. (1)
- Biomet Microfixation, Inc. (1)
How do I get new fdaApprovalPulse: records in Florida by email?
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What are the top fdaApprovalPulse: records in Florida right now?
| Record | Product | Approval | Decided |
|---|---|---|---|
| Lenstec, Inc. | ClearView HD intraocular lens (IOL) | PMA supplement (device change) | 2026-10-23 |
| Cerenovus, Inc. | TRUFILL n-BCA Liquid Embolic System | PMA supplement (device change) | 2026-10-23 |
| Biomet Microfixation, Inc. | Total Temporomandibular Joint Replacement System | PMA supplement (device change) | 2026-07-27 |
| Cordis US Corporation | Exoseal Vascular Closure Device | PMA supplement (device change) | 2026-06-23 |
| Cordis US Corporation | PRECISE PRO RX Nitinol Stent System | PMA supplement (device change) | 2026-06-05 |
| Cordis US Corporation | Cordis Mynx Vascular Closure Portfolio (VCP): MynxGrip, Mynx Control, and Mynx Control Venous Vascular Closure | PMA supplement (device change) | 2026-05-14 |
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)
California (110) Minnesota (61) Massachusetts (37) Oregon (20) Arizona (18) Texas (18) Illinois (9) Maryland (9) Tennessee (8) Pennsylvania (7) 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)
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Frequently asked questions
How many fdaApprovalPulse: records in Florida are listed?
6 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), last refreshed automatically. The most recent is dated 2026-10-23.
Can I get alerts for Florida?
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