Safety lancet (XL) (K262526): 510(k) cleared for Tianjin Huahong Technology Co., Ltd.
Safety lancet (XL) (K262526): 510(k) cleared for Tianjin Huahong Technology Co., Ltd.: 510(k) cleared for Tianjin Huahong Technology Co., Ltd. Its amount of 53 is below the median of 138 (12th percentile). Dated 52 days ago, it serves as a historical benchmark. Score 30/100. As of 2026-11-03, from U.S. FDA openFDA (510(k) clearances and device enforcement reports).
Data as of · Compiled by Zalwin from U.S. FDA openFDA (510(k) clearances and device enforcement reports)
amount: 53 · 12th percentile of 414 FDAPulse records · 0.4x the median
Free preview: all 14 published fields of this record are shown below. Locked: 75 related CN FDAPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Record | 510(k) clearance |
| 510(k) number | K262526 |
| Device | Safety lancet (XL) |
| Applicant | Tianjin Huahong Technology Co., Ltd. |
| Specialty / panel | General, Plastic Surgery |
| Product code | FMK |
| Device class | 2 |
| Clearance type | Traditional |
| Decision | Substantially Equivalent |
| Received | 2026-07-22 |
| Decision date | 2026-09-13 |
| Review time (days) | 53 |
| Third-party review | No |
| Applicant location | Tianjin, CN |
| amount percentile | 12th of 414 (median 138, 0.4x median) |
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CSV columns: Record · Specialty · Date · Review days · Recall class · official source URL
- Source agency: U.S. FDA openFDA (510(k) clearances and device enforcement reports)
- Record date: 2026-09-13
- Data refreshed: 2026-11-03
- Refunds on request within 14 days
Top FDAPulse records (CN first): TECAR Therapy Device (TC2000, TC2001) (K252288) · BreathCare PAP III (YH-390N) (K260251) · Needle Stimulator (SDZ-IIB, SDZ-IIC, SDZ-III, SDZ-V) (K26023 · Mesh Nebulizer (UN204); Mesh Nebulizer (UN205); Mesh Nebuliz · Drainage Catheter (K254179) · Browse all by state and category →
LIVE PUBLIC DATA Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) · Last refreshed: Tue, 03 Nov 2026 18:05:14 GMT
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Peer benchmark and outreach value: Safety lancet (XL) (K262526): 510(k) cleared for Tianjin Huahong Technology Co., Ltd. and 76 CN peers
- CN FDAPulse records like this one: 76
- Safety lancet (XL) (K262526): 510(k) cleared for Tianjin Huahong Technology Co., Ltd.'s amount: 12th percentile of 414 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every CN peer: $15,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
30 / 100 Predicate Speed & CAPA Advisory Opportunity Score
- Fast 53-day review: this device is a strong predicate for similar products.
What is the FDAPulse record for Safety lancet (XL) (K262526): 510(k) cleared for Tianjin Huahong Technology Co., Ltd.?
Safety lancet (XL) (K262526) by Tianjin Huahong Technology Co., Ltd. was cleared on 2026-09-13 after 53 days of review.
How does Safety lancet (XL) (K262526): 510(k) cleared for Tianjin Huahong Technology Co., Ltd. compare to other FDAPulse records?
Its amount of 53 is below the median (12th percentile); smaller records often move faster and face less competition. It is 52 days old; check the official source for later updates before acting. Its Predicate Speed & CAPA Advisory Opportunity Score of 30/100 is modest; treat it as background rather than a priority.
Safety lancet (XL) (K262526) vs. top 3 peers
| Organization | Location | Record date |
|---|---|---|
| Safety lancet (XL) (K262526) | CN | 2026-09-13 |
| TECAR Therapy Device (TC2000, TC2001) (K252288) | CN | 2026-10-13 |
| easyEndo E-Lite Single Use Powered Endoscopic Staplers; easyEndo E-Lite Single Use Powered Endoscopic Staplers with Curved Tip; easyEndo E-Lite Single Use Cartridges (K254291) | CN | 2026-09-25 |
| Nd | CN | 2026-10-13 |
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Recent FDA 510(k) clearances FDA 510(k) clearances and recalls: General & Plastic Surgery devices
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