# Quipment Inc. (repackager or relabeler, Kennesaw, GA): 8 new FDA device listings, incl. set, administration, intravascular

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Quipment Inc. |
| Owner / operator | Quipment Inc |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Kennesaw, GA, US |
| New listings | 8 |
| Devices | Set, Administration, Intravascular; Transmitters And Receivers, Electrocardiograph, Telephone; Set, I.V. Fluid Transfer; Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase; Drug Specific Control Materials; Calibrators, Drug Specific; Dynamometer, Nonpowered; Ventilatory Effort Recorder |
| Product codes | FPA, DXH, LHI, CCJ, LAS, DLJ, HRW, MNR |
| Device classes | Class I, Class II |
| Medical specialties | General Hospital, Cardiovascular, Anesthesiology, Clinical Toxicology, Orthopedic |
| Brand names | Cleo 90 Infusion set; Study Watch; Vented Vial Adapter 20mm; Micro+pro Smokerlyzer; Dynamometer Echo Muscle Tester; WatchPat300 |
| First new listing | 2026-05-12 |
| Latest new listing | 2026-08-25 |
| FDA registration number | 3012302888 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- 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: 2026-10-28T20:51:27.468Z.
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.