DeviceEstablishmentPulse: records in Missouri
11 deviceEstablishmentPulse: records in Missouri are listed from openFDA device registration and listing endpoint (U.S. Food and Drug Administration), dated 2026-05-04 to 2026-10-06; the most frequent is Steris Corporation with 2. Data last updated 2026-10-28; each record links to its official source and a full report.
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
Includes: Establishment, Role, New listings, Devices, Latest listing, official source URL and score · Card, Apple Pay, Google Pay or Link via Stripe
11 records from openFDA device registration and listing endpoint (U.S. Food and Drug Administration), dated 2026-05-04 to 2026-10-06. Most frequent: Steris Corporation (2). Each record links to a full report and the official source.
Last updated 2026-10-28. Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
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- Steris Corporation (2)
- Biomerieux, Inc. (1)
- Surgical Instrument Manufacturers, LLC (1)
- Plus Ev Holdings Inc (1)
- Midwest Sterilization Corp. (1)
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What are the top deviceEstablishmentPulse: records in Missouri right now?
| Record | Role | New listings | Devices |
|---|---|---|---|
| Biomerieux, Inc. | Manufacturer | 11 | Susceptibility Test Cards, Antimicrobial; System, Test, Automated, Antimicrobial Susceptibility, Short Incubation; Panels, Test, Susceptibility, Antimicrobial; Automated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples |
| Surgical Instrument Manufacturers, LLC | Contract manufacturer | 13 | Sacroiliac Joint Fixation; Intervertebral Fusion Device With Bone Graft, Lumbar; Spinal Vertebral Body Replacement Device; Intervertebral Fusion Device With Integrated Fixation, Cervical; Thoracolumbosacral Pedicle Screw System; Appliance, Fixation, Spinal Interlaminal; Intervertebral Fusion Device With Bone Graft, Cervical; Orthosis, Spinal Pedicle Fixation; Orthosis, Spondylolisthesis Spinal Fixation |
| Plus Ev Holdings Inc | Specification developer (outsources manufacturing) | 1 | Massager, Therapeutic, To Internally Massage Trigger Points In The Pelvic Floor Musculature |
| Midwest Sterilization Corp. | Contract sterilizer | 20 | Stimulator, Spinal-Cord, Implanted (Pain Relief); Aortic Valve, Prosthesis, Percutaneously Delivered; Catheter, Ultrasound, Intravascular; Electrode, Spinal Epidural; Catheter, Percutaneous; Prosthesis, Mitral Valve, Percutaneously Delivered; Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation; Cover, Burr Hole; System, Appendage Closure, Left Atrial |
| Bausch & Lomb Incorporated | Manufacturer | 1 | Instrument, Vitreous Aspiration And Cutting, Ac-Powered |
| Steris Corporation | Specification developer (outsources manufacturing) | 1 | Interim Reprocessing Cleaning And Intermediate-Level Disinfection Wipe |
| Pixie Cup LLC | Specification developer (outsources manufacturing) | 1 | Tampon, Menstrual, Unscented |
| Storyup, Inc. Dba Healium | Manufacturer | 1 | Device, Biofeedback |
| STERIS Corporation | Specification developer (outsources manufacturing) | 1 | Retainer, Surgical |
| American Outdoor Brands Products Company | Specification developer (outsources manufacturing) | 1 | Sunglasses (Non-Prescription Including Photosensitive) |
| Steris Corporation | Repackager or relabeler | 1 | Interim Reprocessing Cleaning And Intermediate-Level Disinfection Wipe |
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Manufacturer (1173) Contract manufacturer (527) Specification developer (outsources manufacturing) (336) Repackager or relabeler (192) Foreign exporter (155) Other (93) Contract sterilizer (91) Remanufacturer (3)
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Frequently asked questions
How many deviceEstablishmentPulse: records in Missouri are listed?
11 records from openFDA device registration and listing endpoint (U.S. Food and Drug Administration), last refreshed automatically. The most recent is dated 2026-10-06.
Can I get alerts for Missouri?
Yes. DeviceEstablishmentPulse can email you new records matching this filter; plans are listed on the DeviceEstablishmentPulse page.
Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration). Informational only. RSS feed of new records