# Airicu Inc. (other, City of Industry, CA): 1 new FDA device listing, incl. circuit, breathing (w connector, adaptor, y piece)

**Score:** 35/100

| Field | Value |
|---|---|
| Establishment | Airicu Inc. |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | City of Industry, CA, US |
| New listings | 1 |
| Devices | Circuit, Breathing (W Connector, Adaptor, Y Piece) |
| Product codes | CAI |
| Device classes | Class I |
| Medical specialties | Anesthesiology |
| Brand names | T-Piece: ICU TPH1, ICU TP2, ICU TPH2, ICU TP3, ICU TP5, ICU TPH3, ICU TPH5; Sensor Adapter: ICU SAH22, ICU SA22M, ICU SAH22M; Adapter: ICU NA1, ICU NA2, ICU NAH1, ICU NAH2 |
| First new listing | 2026-08-06 |
| Latest new listing | 2026-08-06 |
| FDA registration number | 3044320625 |
| Registration expires | 2026-12-31 |

## Why this score
- 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: 2026-10-28T20:51:27.468Z.
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.