Chengdu Cryo-Push Medical Technology Co.,Ltd (manufacturer, CHENGDU Sichuan, CN): 4 new FDA device listings, incl. massager, powered inflatable tube
Chengdu Cryo-Push Medical Technology Co.,Ltd (CHENGDU Sichuan): 4 new FDA device listings, incl. massager, powered inflatable tube. Its amount of 4 is above the median of 2 (83rd percentile). Dated 177 days ago, it serves as a historical benchmark. Score 75/100. 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: 4 · 83th percentile of 2,709 DeviceEstablishmentPulse records · 2.0x 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 | Chengdu Cryo-Push Medical Technology Co.,Ltd |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | CHENGDU Sichuan, CN |
| New listings | 4 |
| Devices | Massager, Powered Inflatable Tube; Pack, Hot Or Cold, Water Circulating; Pack, Hot Or Cold, Reusable |
| Product codes | IRP, ILO, IME |
| Device classes | Class I, Class II |
| Medical specialties | Physical Medicine |
| Brand names | Hot and Cold Compression System, MOD: A02-C-032; Cryopush Cold Compression Device, MOD: A02-P-001; RECOVERY+GO Cold Compression Device |
| First new listing | 2026-05-12 |
| Latest new listing | 2026-05-12 |
| FDA registration number | 3011491271 |
| Registration expires | 2026-12-31 |
| amount percentile | 83th of 2,709 (median 2, 2.0x median) |
| Peer records CSV (500 CN 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: 2026-05-12
- 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: Chengdu Cryo-Push Medical Technology Co.,Ltd and 720 CN peers
- CN DeviceEstablishmentPulse records like this one: 720
- Chengdu Cryo-Push Medical Technology Co.,Ltd's amount: 83rd 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)
75 / 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.
What is the DeviceEstablishmentPulse record for Chengdu Cryo-Push Medical Technology Co.,Ltd in CHENGDU Sichuan?
Chengdu Cryo-Push Medical Technology Co.,Ltd (CHENGDU Sichuan, CN), a manufacturer, added 4 FDA device listings on 2026-05-12.
How does Chengdu Cryo-Push Medical Technology Co.,Ltd compare to other DeviceEstablishmentPulse records?
Its amount of 4 sits in the upper half (83th percentile) of 2,709 records; the median is 2. It is 177 days old; check the official source for later updates before acting. Its Score of 75/100 puts it among the stronger signals in this feed.
Chengdu Cryo-Push Medical Technology Co.,Ltd vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Chengdu Cryo-Push Medical Technology Co.,Ltd | CHENGDU Sichuan, CN | 4 | 83rd | 2026-05-12 |
| Applied Medical Resources Corp. | Rsm, CA | 3 | 77th | 2026-10-23 |
| Inter-Med, Inc. | Racine, WI | 5 | 86th | 2026-10-22 |
| Centerpoint Systems LLC | West Valley City, UT | 5 | 86th | 2026-10-21 |
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DeviceEstablishmentPulse: 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.