[DeviceEstablishmentPulse](/v/deviceestablishmentpulse) / compare

# Tornier, Inc. vs St. Jude Medical, Atrial Fibrillation Division, Inc.: DeviceEstablishmentPulse comparison

**Tornier, Inc.'s new listings of 3 is 1.0x St. Jude Medical, Atrial Fibrillation Division, Inc.'s 3 (77th percentile). Tornier, Inc. is dated 2026-10-21; St. Jude Medical, Atrial Fibrillation Division, Inc. 2026-09-18.**

Data as of 2026-11-04 · [Compiled by Zalwin](/research/deviceestablishmentpulse) from openFDA device registration and listing endpoint (U.S. Food and Drug Administration) Copy citation

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## How does Tornier, Inc. compare to St. Jude Medical, Atrial Fibrillation Division, Inc.?

| Field | Tornier, Inc. | St. Jude Medical, Atrial Fibrillation Division, Inc. |
|---|---|---|
| Establishment | Tornier, Inc. | St. Jude Medical, Atrial Fibrillation Division, Inc. |
| Owner / operator | Stryker Corp. | Abbott Laboratories |
| Role | Manufacturer | Manufacturer |
| Establishment types | Manufacture Medical Device; Complaint File Establishment per 21 CFR 820.198 | Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device |
| Location | Bloomington, MN, US | Saint Paul, MN, US |
| New listings | 3 | 3 |
| Devices | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented; Shoulder Prosthesis, Reverse Configuration | Computer, Diagnostic, Programmable |
| Product codes | KWS, PHX | DQK |
| Device classes | Class II | Class II |
| Medical specialties | Orthopedic | Cardiovascular |
| Brand names | Tornier Perform Advanced Glenoid; Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid | EnSite™ X EP System EnSite™ AI Geo Temporary Software License; EnSite™ X EP System EnSite™ AI Geo Software License; EnSite™ X EP System Surface Electrode Kit; EnSite™ X EP System, PFA Index Temporary, Software License; EnSite™ X EP System, PFA Index, Software License; EnSite™ X EP System, Software Upgrade; EnSite™ X EP System, TactiFlex™ Duo Ablation Catheter, Sensor Enabled™, Software License; EnSite™ X EP System, TactiFlex™ Duo Ablation Catheter, Sensor Enabled™ Temporary, Software License |
| First new listing | 2026-09-30 | 2026-05-21 |
| Latest new listing | 2026-10-21 | 2026-09-18 |
| FDA registration number | 1649390 | 2184149 |
| Registration expires | 2027-12-31 | 2027-12-31 |
| amount percentile | 77th | 77th |
| Score | 95/100 | 85/100 |
| Peer rank and all 45 MN records (CSV) | Every comparable record ranked, with amounts, dates and scores 🔒 Click to unlock → |
| Official source URLs for every peer record | Direct links to each record at its government source 🔒 Click to unlock → |

Official records: [Tornier, Inc.](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm) · [St. Jude Medical, Atrial Fibrillation Division, Inc.](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm)

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