FdaApprovalPulse: records in Maryland
9 fdaApprovalPulse: records in Maryland are listed from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-06-22 to 2026-10-16; the most frequent is Lung Bioengineering, Inc. 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
9 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-06-22 to 2026-10-16. Most frequent: Lung Bioengineering, Inc. (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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- Lung Bioengineering, Inc. (3)
- Becton, Dickinson and Company (2)
- Personal Genome Diagnostics, Inc. (1)
- Life Technologies Corporation (1)
- Terumo Medical Corporation (1)
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What are the top fdaApprovalPulse: records in Maryland right now?
| Record | Product | Approval | Decided |
|---|---|---|---|
| Lung Bioengineering, Inc. | LungFX Device | PMA supplement (device change) | 2026-10-16 |
| Lung Bioengineering, Inc. | LungFX Device | PMA supplement (device change) | 2026-10-16 |
| Personal Genome Diagnostics, Inc. | PGDx elio tissue complete CDx | PMA original approval (new class III device) | 2026-07-30 |
| Lung Bioengineering, Inc. | LungFX device | PMA original approval (new class III device) | 2026-06-22 |
| Life Technologies Corporation | Oncomine Dx Express Test | PMA supplement (device change) | 2026-09-09 |
| Becton, Dickinson and Company | BD Onclarity HPV Assay Reagent Pack (SKU 444075) and BD COR HPV Extraction Trough (SKU 444074) | PMA supplement (device change) | 2026-08-19 |
| Becton, Dickinson and Company | BD Onclarity HPV Assay | PMA supplement (device change) | 2026-08-14 |
| Terumo Medical Corporation | Angio Seal VIP Vascular Closure Device | PMA supplement (device change) | 2026-08-04 |
| Dt Medtech, LLC | Hintermann Series H3 Total Ankle Replacement System | PMA supplement (device change) | 2026-07-31 |
Which related categories and locations should I check?
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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)
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Frequently asked questions
How many fdaApprovalPulse: records in Maryland are listed?
9 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), last refreshed automatically. The most recent is dated 2026-10-16.
Can I get alerts for Maryland?
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