# Sequitur Health Corp. (manufacturer, Phoenix, AZ): 3 new FDA device listings, incl. analyzer, chemistry (photometric, discrete), for clinical use

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Sequitur Health Corp. |
| Role | Manufacturer |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device |
| Location | Phoenix, AZ, US |
| New listings | 3 |
| Devices | Analyzer, Chemistry (Photometric, Discrete), For Clinical Use; Photometric Method, Ammonia; Single (Specified) Analyte Controls (Assayed And Unassayed) |
| Product codes | JJE, JID, JJX |
| Device classes | Class I |
| Medical specialties | Clinical Chemistry |
| Brand names | AMI; AMI Plasma Cartridge; AMI QC Level 2; AMI QC Level 1 |
| First new listing | 2026-09-02 |
| Latest new listing | 2026-09-02 |
| FDA registration number | 3023591031 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.