Katecho LLC (contract manufacturer, Des Moines, IA): 2 new FDA device listings, incl. temporarily implanted peripheral nerve stimulation system for sustaine
Katecho LLC (Des Moines, Iowa): 2 new FDA device listings, incl. temporarily implanted peripheral nerve stimulation system for sustaine. Its amount of 2 is above the median of 1 (69th percentile). Dated 111 days ago, it serves as a historical benchmark. Score 65/100. 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: 2 · 69th percentile of 2,570 DeviceEstablishmentPulse records · 2.0x the median
Free preview: all 13 published fields of this record are shown below. Locked: 1 related IA DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Katecho LLC |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Des Moines, IA, US |
| New listings | 2 |
| Devices | Temporarily Implanted Peripheral Nerve Stimulation System For Sustained Pain Relief; Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief |
| Product codes | SCN, NHI |
| Device classes | Class II |
| Medical specialties | Neurology |
| First new listing | 2026-05-08 |
| Latest new listing | 2026-07-17 |
| FDA registration number | 1930027 |
| Registration expires | 2027-12-31 |
| amount percentile | 69th of 2,570 (median 1, 2.0x median) |
| Peer records CSV (2 IA 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: 2026-07-17
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (IA first): Titanlinks Logistics LLC (repackager or relabeler, Newark, D · Millstone Medical Outsourcing LLC (contract manufacturer, Ol · Soher Med Limited (foreign exporter, Hong Kong, HK) · Icu Medical, Inc. (specification developer, San Clemente, CA · MEDLINE INDUSTRIES, LP - Northfield (specification developer · 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: Katecho LLC and 2 Iowa peers
- Iowa DeviceEstablishmentPulse records like this one: 2
- Katecho LLC's amount: 69th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Iowa peer: $400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
65 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Katecho LLC in Des Moines, Iowa?
Katecho LLC (Des Moines, IA), a contract manufacturer, added 2 FDA device listings between 2026-05-08 and 2026-07-17.
How does Katecho LLC compare to other Iowa DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 111 days old; check the official source for later updates before acting.
Katecho LLC vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Katecho LLC | Des Moines, IA | 2 | 69th | 2026-07-17 |
| Tecomet Inc. | Wilmington, MA | 3 | 77th | 2026-10-15 |
| Bard Shannon Limited | Humacao, PR | 3 | 77th | 2026-10-14 |
| Orchid Orthopedic Solutions Oregon, Inc. | Oregon City, OR | 3 | 77th | 2026-10-05 |
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.