Vessel Closure Device (VCD177213P) (K260677): 510(k) cleared for Vcd Medical S.R.L.
Vessel Closure Device (VCD177213P) (K260677): 510(k) cleared for Vcd Medical S.R.L.: 510(k) cleared for Vcd Medical S.R.L. Its amount of 199 is above the median of 138 (68th percentile). Dated 48 days ago, it serves as a historical benchmark. Score 42/100. As of 2026-11-04, 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: 199 · 68th percentile of 414 FDAPulse records · 1.4x the median
Free preview: all 14 published fields of this record are shown below. Locked: 5 related IT FDAPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Record | 510(k) clearance |
| 510(k) number | K260677 |
| Device | Vessel Closure Device (VCD177213P) |
| Applicant | Vcd Medical S.R.L. |
| Specialty / panel | General, Plastic Surgery |
| Product code | FZP |
| Device class | 2 |
| Clearance type | Traditional |
| Decision | Substantially Equivalent |
| Received | 2026-03-02 |
| Decision date | 2026-09-17 |
| Review time (days) | 199 |
| Third-party review | No |
| Applicant location | Brescia, IT |
| amount percentile | 68th of 414 (median 138, 1.4x 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: 2026-09-17
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
Top FDAPulse records (IT first): Digistat Care (K261287) · HORIZON 8AF (Integrated OXY MODULE 8AF and Horizon CVR) (US5 · Plenity-V (MC0979 / GS110) (K261783) · Tri Stage Venous Cannulae (K262052) · Dual Stage Venous Cannulae (K263092) · Browse all by state and category →
LIVE PUBLIC DATA Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) · Last refreshed: Wed, 04 Nov 2026 09:16:12 GMT
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Peer benchmark and outreach value: Vessel Closure Device (VCD177213P) (K260677): 510(k) cleared for Vcd Medical S.R.L. and 6 IT peers
- IT FDAPulse records like this one: 6
- Vessel Closure Device (VCD177213P) (K260677): 510(k) cleared for Vcd Medical S.R.L.'s amount: 68th percentile of 414 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every IT peer: $1,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
42 / 100 Predicate Speed & CAPA Advisory Opportunity Score
- 199-day review, longer than typical.
What is the FDAPulse record for Vessel Closure Device (VCD177213P) (K260677): 510(k) cleared for Vcd Medical S.R.L.?
Vessel Closure Device (VCD177213P) (K260677) by Vcd Medical S.R.L. was cleared on 2026-09-17 after 199 days of review.
How does Vessel Closure Device (VCD177213P) (K260677): 510(k) cleared for Vcd Medical S.R.L. compare to other FDAPulse records?
Its amount of 199 sits in the upper half (68th percentile) of 414 records; the median is 138. It is 48 days old; check the official source for later updates before acting.
Vessel Closure Device (VCD177213P) (K260677) vs. top 3 peers
| Organization | Location | Record date |
|---|---|---|
| Vessel Closure Device (VCD177213P) (K260677) | IT | 2026-09-17 |
| 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 |
| PicoreMax (PicoreMax) (K254199) | KR | 2026-09-24 |
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