Stryker Puerto Rico, LLC. (contract manufacturer, Arroyo, PR): 4 new FDA device listings, incl. nasopharyngoscope (flexible or rigid)
Stryker Puerto Rico, LLC. (Arroyo, Puerto Rico): 4 new FDA device listings, incl. nasopharyngoscope (flexible or rigid). Its amount of 4 is above the median of 1 (83rd percentile). Dated 136 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: 4 · 83th percentile of 2,570 DeviceEstablishmentPulse records · 4.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 6 related PR DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Stryker Puerto Rico, LLC. |
| Owner / operator | Stryker Corp. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Arroyo, PR, US |
| New listings | 4 |
| Devices | Nasopharyngoscope (Flexible Or Rigid); Endoscope, Neurological; Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece |
| Product codes | EOB, GWG, ERL |
| Device classes | Class II |
| Medical specialties | Ear, Nose, Throat, Neurology |
| Brand names | Hydro Irrigation Console; Hydro Disposable Irrigation Cassette; Hydro Foot Switch |
| First new listing | 2026-05-26 |
| Latest new listing | 2026-06-22 |
| FDA registration number | 2648666 |
| Registration expires | 2027-12-31 |
| amount percentile | 83th of 2,570 (median 1, 4.0x median) |
| Peer records CSV (7 PR 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: 2026-06-22
- 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: Stryker Puerto Rico, LLC. and 7 Puerto Rico peers
- Puerto Rico DeviceEstablishmentPulse records like this one: 7
- Stryker Puerto Rico, LLC.'s amount: 83rd percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Puerto Rico peer: $1,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
80 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Stryker Puerto Rico, LLC. in Arroyo, Puerto Rico?
Stryker Puerto Rico, LLC. (Arroyo, PR), a contract manufacturer, added 4 FDA device listings between 2026-05-26 and 2026-06-22.
How does Stryker Puerto Rico, LLC. compare to other Puerto Rico DeviceEstablishmentPulse records?
Its amount of 4 sits in the upper half (83th percentile) of 2,570 records; the median is 1. It is 136 days old; check the official source for later updates before acting. Its Score of 80/100 puts it among the stronger signals in this feed.
Stryker Puerto Rico, LLC. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Stryker Puerto Rico, LLC. | Arroyo, PR | 4 | 83rd | 2026-06-22 |
| NGInstruments, Inc dba Avalign Cutting Instruments | Warsaw, IN | 4 | 83rd | 2026-10-16 |
| Cook Medical LLC | Bloomington, IN | 4 | 83rd | 2026-10-13 |
| Swiss-American CDMO,LLC | Carrollton, TX | 4 | 83rd | 2026-10-12 |
Related records
DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: U.S. establishment
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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.