Amphenol Medical Technologies (Dongguan) Co., Ltd. (contract manufacturer, Dongguan Guangdong, CN): 2 new FDA device listings, incl. computer, diagnostic, programmable
Amphenol Medical Technologies (Dongguan) Co., Ltd. (Dongguan Guangdong): 2 new FDA device listings, incl. computer, diagnostic, programmable. Its amount of 2 is above the median of 2 (69th percentile). Dated 80 days ago, it serves as a historical benchmark. Score 55/100. 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: 2 · 69th percentile of 2,709 DeviceEstablishmentPulse records · 1.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Amphenol Medical Technologies (Dongguan) Co., Ltd. |
| Owner / operator | Amphenol Critical Medical Technologies, LLC |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Dongguan Guangdong, CN |
| New listings | 2 |
| Devices | Computer, Diagnostic, Programmable; Cable, Transducer And Electrode, Patient, (Including Connector) |
| Product codes | DQK, DSA |
| Device classes | Class II |
| Medical specialties | Cardiovascular |
| Brand names | IBP cable |
| First new listing | 2026-08-11 |
| Latest new listing | 2026-08-17 |
| FDA registration number | 3013596024 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,709 (median 2, 1.0x median) |
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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: 2026-08-17
- 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: Amphenol Medical Technologies (Dongguan) Co., Ltd. and 720 CN peers
- CN DeviceEstablishmentPulse records like this one: 720
- Amphenol Medical Technologies (Dongguan) Co., Ltd.'s amount: 69th 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)
55 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
What is the DeviceEstablishmentPulse record for Amphenol Medical Technologies (Dongguan) Co., Ltd. in Dongguan Guangdong?
Amphenol Medical Technologies (Dongguan) Co., Ltd. (Dongguan Guangdong, CN), a contract manufacturer, added 2 FDA device listings between 2026-08-11 and 2026-08-17.
How does Amphenol Medical Technologies (Dongguan) Co., Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,709 records; the median is 2. It is 80 days old; check the official source for later updates before acting.
Amphenol Medical Technologies (Dongguan) Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan Guangdong, CN | 2 | 69th | 2026-08-17 |
| 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 |
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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.