Tornier, Inc. (manufacturer, Bloomington, MN): 1 new FDA device listing, incl. prosthesis, shoulder, semi-constrained, metal/polymer cemented
Tornier, Inc. (Bloomington, Minnesota): 1 new FDA device listing, incl. prosthesis, shoulder, semi-constrained, metal/polymer cemented. Its amount of 1 is above the median of 1 (50th percentile). Dated 36 days ago, it serves as a historical benchmark. Score 80/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 1 · 50th percentile of 2,570 DeviceEstablishmentPulse records · 1.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 42 related MN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Tornier, Inc. |
| Owner / operator | Stryker Corp. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device; Complaint File Establishment per 21 CFR 820.198 |
| Location | Bloomington, MN, US |
| New listings | 1 |
| Devices | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented |
| Product codes | KWS |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | Tornier Perform Advanced Glenoid |
| First new listing | 2026-09-30 |
| Latest new listing | 2026-09-30 |
| FDA registration number | 1649390 |
| Registration expires | 2027-12-31 |
| amount percentile | 50th of 2,570 (median 1, 1.0x median) |
| Peer records CSV (43 MN records) | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-09-30
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (MN first): Boston Scientific Corporation (manufacturer, Saint Paul, MN) · EPIC MedTec OEM Catheter & Wire LLC (contract manufacturer, · Isomedix Operations, Inc. (contract sterilizer, Minneapolis, · Rms Co. (contract manufacturer, Minneapolis, MN) · Boston Scientific Corporation (specification developer, Mapl · Browse all by state and category →
LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Tornier, Inc. and 43 Minnesota peers
- Minnesota DeviceEstablishmentPulse records like this one: 43
- Tornier, Inc.'s amount: 50th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Minnesota peer: $8,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
80 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Tornier, Inc. in Bloomington, Minnesota?
Tornier, Inc. (Bloomington, MN), a manufacturer, added 1 FDA device listing on 2026-09-30.
How does Tornier, Inc. compare to other Minnesota DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,570 records; the median is 1. It is 36 days old, still within a typical 45-day follow-up window. Its Score of 80/100 puts it among the stronger signals in this feed.
Tornier, Inc. vs. top 2 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Tornier, Inc. | Bloomington, MN | 1 | 50th | 2026-09-30 |
| Piraeus Medical, Inc. | Maple Grove, MN | 4 | 83rd | 2026-10-12 |
| Boston Scientific Corporation | Saint Paul, MN | 24 | 98th | 2026-10-16 |
Related records
DeviceEstablishmentPulse: Manufacturer DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Minnesota
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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.