Guangdong Hexin Technology Weaving Co., LTD (contract manufacturer, Huizhou City Guangdong, CN): 1 new FDA device listing, incl. sling, arm, overhead supported
Guangdong Hexin Technology Weaving Co., LTD (Huizhou City Guangdong): 1 new FDA device listing, incl. sling, arm, overhead supported. Its amount of 1 is above the median of 2 (50th percentile). Dated 51 days ago, it serves as a historical benchmark. Score 40/100. As of 2026-11-04, 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 2,709 DeviceEstablishmentPulse records · 0.5x the median
Free preview: all 14 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Guangdong Hexin Technology Weaving Co., LTD |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Huizhou City Guangdong, CN |
| New listings | 1 |
| Devices | Sling, Arm, Overhead Supported |
| Product codes | ILE |
| Device classes | Class I |
| Medical specialties | Physical Medicine |
| Brand names | Norco:Shoulder Immobilizer- Large with Model NC16018-3; Norco:Shoulder Immobilizer- X large with Model NC16018-4; Norco:Shoulder Immobilizer- Small with Model NC16018-1; Norco:Shoulder Immobilizer- Medium with Model NC16018-2 |
| First new listing | 2026-09-15 |
| Latest new listing | 2026-09-15 |
| FDA registration number | 3009759417 |
| Registration expires | 2026-12-31 |
| amount percentile | 50th of 2,709 (median 2, 0.5x median) |
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| 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: 2026-09-15
- Data refreshed: 2026-11-04
- 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, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Guangdong Hexin Technology Weaving Co., LTD and 720 CN peers
- CN DeviceEstablishmentPulse records like this one: 720
- Guangdong Hexin Technology Weaving Co., LTD's amount: 50th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every CN peer: $144,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
40 / 100 Score
- Contract manufacturer or sterilizer adding work.
What is the DeviceEstablishmentPulse record for Guangdong Hexin Technology Weaving Co., LTD in Huizhou City Guangdong?
Guangdong Hexin Technology Weaving Co., LTD (Huizhou City Guangdong, CN), a contract manufacturer, added 1 FDA device listing on 2026-09-15.
How does Guangdong Hexin Technology Weaving Co., LTD compare to other DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,709 records; the median is 2. It is 51 days old; check the official source for later updates before acting.
Guangdong Hexin Technology Weaving Co., LTD vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Guangdong Hexin Technology Weaving Co., LTD | Huizhou City Guangdong, CN | 1 | 50th | 2026-09-15 |
| 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
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- Millstone Medical Outsourcing LLC.
- Karl Storz Endoscopy-America, Inc.
- Orchid Orthopedic Solutions Oregon, Inc.
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DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: Foreign 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.