Peter's Technology (Suzhou) Co., Ltd. (contract manufacturer, Suzhou Jiangsu, CN): 9 new FDA device listings, incl. electrosurgical, cutting & coagulation & accessories
Peter's Technology (Suzhou) Co., Ltd. (Suzhou Jiangsu): 9 new FDA device listings, incl. electrosurgical, cutting & coagulation & accessories. Its amount of 9 is top-decile (92nd percentile of 2,570 records). Dated 22 days ago, it is in the active follow-up window. Score 80/100. 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: 9 · 92th percentile of 2,570 DeviceEstablishmentPulse records · 9.0x 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 | Peter's Technology (Suzhou) Co., Ltd. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Suzhou Jiangsu, CN |
| New listings | 9 |
| Devices | Electrosurgical, Cutting & Coagulation & Accessories; Arthroscope; Eyelid Thermal Pulsation System; Evacuator, Gastro-Urology; Resectoscope; Trabeculotome; Pump, Infusion, Ophthalmic |
| Product codes | GEI, HRX, ORZ, KQT, FJL, HMZ, MRH |
| Device classes | Class I, Class II |
| Medical specialties | General, Plastic Surgery, Orthopedic, Ophthalmic, Gastroenterology, Urology, General Hospital |
| Brand names | Legato®, Vaporflex®; Tricera Arthroscopic System |
| First new listing | 2026-08-05 |
| Latest new listing | 2026-10-14 |
| FDA registration number | 3007113251 |
| Registration expires | 2027-12-31 |
| amount percentile | 92th of 2,570 (median 1, 9.0x median) |
| Peer records CSV (500 CN records) | 🔒 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: 2026-10-14
- Data refreshed: 2026-10-28
- 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, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Peter's Technology (Suzhou) Co., Ltd. and 687 CN peers
- CN DeviceEstablishmentPulse records like this one: 687
- Peter's Technology (Suzhou) Co., Ltd.'s amount: 92nd percentile of 2,570 records
- Timing: Medium: dated in the last 30 days
- Estimated pipeline if you contact every CN peer: $137,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
80 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Peter's Technology (Suzhou) Co., Ltd. in Suzhou Jiangsu?
Peter's Technology (Suzhou) Co., Ltd. (Suzhou Jiangsu, CN), a contract manufacturer, added 9 FDA device listings between 2026-08-05 and 2026-10-14.
How does Peter's Technology (Suzhou) Co., Ltd. compare to other DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 9 is 9.0x the median of 1 across 2,570 records. It is 22 days old, still within a typical 45-day follow-up window. Its Score of 80/100 puts it among the stronger signals in this feed.
Peter's Technology (Suzhou) Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Peter's Technology (Suzhou) Co., Ltd. | Suzhou Jiangsu, CN | 9 | 92nd | 2026-10-14 |
| Arthrex, Inc. | Ave Maria, FL | 10 | 93rd | 2026-09-27 |
| Biopro, Inc. | Port Huron, MI | 11 | 94th | 2026-10-15 |
| NGInstruments, Inc dba Avalign Cutting Instruments | Warsaw, IN | 4 | 83rd | 2026-10-16 |
Related records
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.