# Moebius Precision Corp (contract manufacturer, Lansing, MI): 4 new FDA device listings, incl. prosthesis, knee, patellofemorotibial, semi-constrained, cemented, pol

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Moebius Precision Corp |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Lansing, MI, US |
| New listings | 4 |
| Devices | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer; Fastener, Fixation, Nondegradable, Soft Tissue |
| Product codes | JWH, MBH, MBI |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | Modular Knee System; CKS, RPL Femoral Component; Threaded anchor |
| First new listing | 2026-08-04 |
| Latest new listing | 2026-08-04 |
| FDA registration number | 3021902344 |
| 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.