Weifang Keepbetter Healthcare Co., Ltd. (manufacturer, Weifang Shandong, CN): 5 new FDA device listings, incl. fiber, medical, absorbent
Weifang Keepbetter Healthcare Co., Ltd. (Weifang Shandong): 5 new FDA device listings, incl. fiber, medical, absorbent. Its amount of 5 is above the median of 1 (87th percentile). Dated 78 days ago, it serves as a historical benchmark. Score 60/100. 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: 5 · 87th percentile of 2,570 DeviceEstablishmentPulse records · 5.0x 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 | Weifang Keepbetter Healthcare Co., Ltd. |
| Owner / operator | Weifang KeepBetter Healthcare Co., Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Weifang Shandong, CN |
| New listings | 5 |
| Devices | Fiber, Medical, Absorbent; Disinfectant, Medical Devices; Garment, Protective, For Incontinence; Pad, Menstrual, Unscented; Cover, Mattress (Medical Purposes) |
| Product codes | FRL, LRJ, EYQ, HHD, FMW |
| Device classes | Class I |
| Medical specialties | General Hospital, Gastroenterology, Urology, Obstetrics/Gynecology |
| Brand names | Disposable pet training pad; Disposable dry wipe; Disposable baby wet wipe; Disposable household wet wipe; Disposable wet wipe; Disposable pet diaper; Disposable baby diaper; Disposable baby pull up |
| First new listing | 2026-08-19 |
| Latest new listing | 2026-08-19 |
| FDA registration number | 3022968389 |
| Registration expires | 2026-12-31 |
| amount percentile | 87th of 2,570 (median 1, 5.0x 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: 2026-08-19
- 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: Weifang Keepbetter Healthcare Co., Ltd. and 687 CN peers
- CN DeviceEstablishmentPulse records like this one: 687
- Weifang Keepbetter Healthcare Co., Ltd.'s amount: 87th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every CN peer: $137,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
60 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Weifang Keepbetter Healthcare Co., Ltd. in Weifang Shandong?
Weifang Keepbetter Healthcare Co., Ltd. (Weifang Shandong, CN), a manufacturer, added 5 FDA device listings on 2026-08-19.
How does Weifang Keepbetter Healthcare Co., Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 5 sits in the upper half (87th percentile) of 2,570 records; the median is 1. It is 78 days old; check the official source for later updates before acting.
Weifang Keepbetter Healthcare Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Weifang Keepbetter Healthcare Co., Ltd. | Weifang Shandong, CN | 5 | 87th | 2026-08-19 |
| Inquis Medical, Inc. | Menlo Park, CA | 5 | 87th | 2026-10-16 |
| Boston Scientific Corp., Marina Bay Cust. Fulfillment Center | Quincy, MA | 6 | 88th | 2026-10-16 |
| Piraeus Medical, Inc. | Maple Grove, MN | 4 | 83rd | 2026-10-12 |
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.