Depuy Synthes (Suzhou) Medical Devices Co., Ltd. (manufacturer, SUZHOU Jiangsu, CN): 2 new FDA device listings, incl. prosthesis, knee, patellofemorotibial, semi-constrained, cemented, pol
Depuy Synthes (Suzhou) Medical Devices Co., Ltd. (SUZHOU Jiangsu): 2 new FDA device listings, incl. prosthesis, knee, patellofemorotibial, semi-constrained, cemented, pol. Its amount of 2 is above the median of 2 (69th percentile). Dated 42 days ago, it serves as a historical benchmark. Score 70/100. 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 14 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Depuy Synthes (Suzhou) Medical Devices Co., Ltd. |
| Owner / operator | DePuy Synthes, Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | SUZHOU Jiangsu, CN |
| New listings | 2 |
| Devices | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
| Product codes | OIY, JWH |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| First new listing | 2026-09-24 |
| Latest new listing | 2026-09-24 |
| FDA registration number | 3006356043 |
| Registration expires | 2027-12-31 |
| 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: 2026-09-24
- 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: Depuy Synthes (Suzhou) Medical Devices Co., Ltd. and 720 CN peers
- CN DeviceEstablishmentPulse records like this one: 720
- Depuy Synthes (Suzhou) Medical Devices 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)
70 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Depuy Synthes (Suzhou) Medical Devices Co., Ltd. in SUZHOU Jiangsu?
Depuy Synthes (Suzhou) Medical Devices Co., Ltd. (SUZHOU Jiangsu, CN), a manufacturer, added 2 FDA device listings on 2026-09-24.
How does Depuy Synthes (Suzhou) Medical Devices 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 42 days old, still within a typical 45-day follow-up window. Its Score of 70/100 puts it among the stronger signals in this feed.
Depuy Synthes (Suzhou) Medical Devices Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Depuy Synthes (Suzhou) Medical Devices Co., Ltd. | SUZHOU Jiangsu, CN | 2 | 69th | 2026-09-24 |
| Applied Medical Resources Corp. | Rsm, CA | 3 | 77th | 2026-10-23 |
| Tornier, Inc. | Bloomington, MN | 3 | 77th | 2026-10-21 |
| Treace Medical Concepts, Inc. | Ponte Vedra, FL | 3 | 77th | 2026-10-20 |
Related records
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- Tornier, Inc.
- Treace Medical Concepts, Inc.
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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.