# Zigg Design LLC (contract manufacturer, Nibley, UT): 33 new FDA device listings, incl. intervertebral fusion device with integrated fixation, cervical

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Zigg Design LLC |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Nibley, UT, US |
| New listings | 33 |
| Devices | Intervertebral Fusion Device With Integrated Fixation, Cervical; Intervertebral Fusion Device With Bone Graft, Cervical; Posterior Cervical Screw System; Appliance, Fixation, Spinal Interlaminal; Orthosis, Spine, Plate, Laminoplasty, Metal; Appliance, Fixation, Spinal Intervertebral Body; Spinal Vertebral Body Replacement Device; Intervertebral Fusion Device With Bone Graft, Lumbar; Thoracolumbosacral Pedicle Screw System; Sacroiliac Joint Fixation |
| Product codes | OVE, ODP, NKG, KWP, NQW, KWQ, MQP, MAX, NKB, OUR, OVD, MRW |
| Device classes | Class II, Unclassified |
| Medical specialties | Orthopedic |
| Brand names | ClariVy Cervical IBF System; ClariVy NanoVy Ti Cervical IBF System; ClariVy OsteoVy PEKK Cervical IBF System; VySpan PCT System; UniVy OsteoVy Ti NanoVy HA Cervical IBF System; UniVy OsteoVy Cervical IBF System; VyLam Laminoplasty System; VyPlate Anterior Cervical Plate System |
| First new listing | 2026-09-21 |
| Latest new listing | 2026-09-21 |
| FDA registration number | 3009957608 |
| 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.