Rens Medcare (Cambodia) Co.,Ltd. (manufacturer, Sihanouk Preah Sihanouk, KH): 3 new FDA device listings, incl. system, measurement, blood-pressure, non-invasive
Rens Medcare (Cambodia) Co.,Ltd. (Sihanouk Preah Sihanouk): 3 new FDA device listings, incl. system, measurement, blood-pressure, non-invasive. Its amount of 3 is above the median of 1 (77th percentile). Dated 65 days ago, it serves as a historical benchmark. Score 75/100. 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: 3 · 77th percentile of 2,570 DeviceEstablishmentPulse records · 3.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 9 related KH DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Rens Medcare (Cambodia) Co.,Ltd. |
| Owner / operator | Joytech Healthcare Co. Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Sihanouk Preah Sihanouk, KH |
| New listings | 3 |
| Devices | System, Measurement, Blood-Pressure, Non-Invasive |
| Product codes | DXN |
| Device classes | Class II |
| Medical specialties | Cardiovascular |
| Brand names | Arm-type Fully Automatic Digital Blood Pressure Monitor; Blood Pressure Monitor 16-1991; Blood pressure monitor; DBP-6196-P Blood Pressure Monitor; Blood Pressure Monitor 16-1993XL |
| First new listing | 2026-05-07 |
| Latest new listing | 2026-09-01 |
| FDA registration number | 3024790242 |
| Registration expires | 2027-12-31 |
| amount percentile | 77th of 2,570 (median 1, 3.0x median) |
| Peer records CSV (10 KH 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: 2026-09-01
- 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: Rens Medcare (Cambodia) Co.,Ltd. and 10 KH peers
- KH DeviceEstablishmentPulse records like this one: 10
- Rens Medcare (Cambodia) Co.,Ltd.'s amount: 77th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every KH peer: $2,000 (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 Rens Medcare (Cambodia) Co.,Ltd. in Sihanouk Preah Sihanouk?
Rens Medcare (Cambodia) Co.,Ltd. (Sihanouk Preah Sihanouk, KH), a manufacturer, added 3 FDA device listings between 2026-05-07 and 2026-09-01.
How does Rens Medcare (Cambodia) Co.,Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 3 sits in the upper half (77th percentile) of 2,570 records; the median is 1. It is 65 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.
Rens Medcare (Cambodia) Co.,Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Rens Medcare (Cambodia) Co.,Ltd. | Sihanouk Preah Sihanouk, KH | 3 | 77th | 2026-09-01 |
| Beacon Biosignals, Inc. | Boston, MA | 3 | 77th | 2026-10-16 |
| Endovascular Engineering, Inc. | Menlo Park, CA | 3 | 77th | 2026-10-14 |
| INNO Holdings Inc. | Millcreek, UT | 3 | 77th | 2026-10-05 |
Related records
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.