# Shanghai Jpy Ion-Tech Co., Ltd. (contract sterilizer, Shanghai, CN): 16 new FDA device listings, incl. prosthesis, hip, semi-constrained, metal/polymer, porous uncemented

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Shanghai Jpy Ion-Tech Co., Ltd. |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer) |
| Location | Shanghai, CN |
| New listings | 16 |
| Devices | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish; Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented; Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate; Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer; Prosthesis, Total Anatomic Shoulder, Uncemented Metaphyseal Humeral Stem With No Diaphyseal Incursion, Semi-Constrained; Resin, Root Canal Filling; Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented; Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented |
| Product codes | LPH, KWY, MAY, OQG, MEH, KWZ, PKC, KIF, HSD, KWS, PHX, OIY, JWH, MBH, HMZ |
| Device classes | Class I, Class II |
| Medical specialties | Orthopedic, Dental, Ophthalmic, General Hospital |
| Brand names | Taperloc Complete Hip Stem; GLOBAL ICON; PINNACLE GRIPTION; GLOBAL UNITE; ATTUNE; OMNI Ultra Surgical System |
| First new listing | 2026-08-11 |
| Latest new listing | 2026-08-11 |
| FDA registration number | 3004748528 |
| 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.

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.