DeviceEstablishmentPulse / report
Arthrex, Inc. (specification developer, Naples, FL): 12 new FDA device listings, incl. screw, fixation, bone
Arthrex, Inc. (Naples, Florida): 12 new FDA device listings, incl. screw, fixation, bone. Its amount of 12 is top-decile (95th percentile of 2,570 records). Dated 38 days ago, it serves as a historical benchmark. Score 95/100. 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: 12 · 95th percentile of 2,570 DeviceEstablishmentPulse records · 12.0x the median
Free preview: all 13 published fields of this record are shown below. Locked: 83 related FL DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Arthrex, Inc. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility |
| Location | Naples, FL, US |
| New listings | 12 |
| Devices | Screw, Fixation, Bone; Fastener, Fixation, Biodegradable, Soft Tissue; Staple, Fixation, Bone; Fastener, Fixation, Nondegradable, Soft Tissue; Prosthesis, Elbow, Hemi-, Radial, Polymer; System, Facet Screw Spinal Device |
| Product codes | HWC, MAI, JDR, MBI, KWI, MRW |
| Device classes | Class II, Unclassified |
| Medical specialties | Orthopedic |
| First new listing | 2026-05-11 |
| Latest new listing | 2026-09-27 |
| FDA registration number | 1220246 |
| Registration expires | 2027-12-31 |
| amount percentile | 95th of 2,570 (median 1, 12.0x median) |
| Peer records CSV (84 FL records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 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: 2026-09-27
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
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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: Arthrex, Inc. and 84 Florida peers
- Florida DeviceEstablishmentPulse records like this one: 84
- Arthrex, Inc.'s amount: 95th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Florida peer: $16,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
95 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Arthrex, Inc. in Naples, Florida?
Arthrex, Inc. (Naples, FL), a specification developer (outsources manufacturing), added 12 FDA device listings between 2026-05-11 and 2026-09-27.
How does Arthrex, Inc. compare to other Florida DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 12 is 12.0x the median of 1 across 2,570 records. It is 38 days old, still within a typical 45-day follow-up window. Its Score of 95/100 puts it among the stronger signals in this feed.
Arthrex, Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Arthrex, Inc. | Naples, FL | 12 | 95th | 2026-09-27 |
| Glownar Aesthetics. LLC | Davie, FL | 10 | 93rd | 2026-09-24 |
| Boston Scientific Corporation | Marlborough, MA | 9 | 92nd | 2026-10-16 |
| Sol-Millennium Medical, Inc. | Chicago, IL | 8 | 91st | 2026-09-28 |
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DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Florida
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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.