# Curiteva, Inc. (contract manufacturer, Tanner, AL): 11 new FDA device listings, incl. appliance, fixation, spinal intervertebral body

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Curiteva, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Tanner, AL, US |
| New listings | 11 |
| Devices | Appliance, Fixation, Spinal Intervertebral Body; Orthopedic Stereotaxic Instrument; Retractor; Intervertebral Fusion Device With Bone Graft, Lumbar; Intervertebral Fusion Device With Integrated Fixation, Lumbar; Intervertebral Fusion Device With Bone Graft, Thoracic; Gauge, Depth |
| Product codes | KWQ, OLO, GAD, MAX, OVD, PHM, HTJ |
| Device classes | Class I, Class II |
| Medical specialties | Orthopedic, Neurology, General, Plastic Surgery |
| Brand names | N/A |
| First new listing | 2026-08-10 |
| Latest new listing | 2026-09-04 |
| FDA registration number | 3012131184 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- 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: 2026-11-04T21:52:36.524Z.
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.