# Durashield Device Kit (K252995): 510(k) cleared for SurGenTec, LLC

**Predicate Speed & CAPA Advisory Opportunity Score:** 55/100

| Field | Value |
|---|---|
| Record | 510(k) clearance |
| 510(k) number | K252995 |
| Device | Durashield Device Kit |
| Applicant | SurGenTec, LLC |
| Specialty / panel | Neurology |
| Product code | GZT |
| Device class | 2 |
| Clearance type | Traditional |
| Decision | Substantially Equivalent |
| Received | 2025-09-18 |
| Decision date | 2026-09-17 |
| Review time (days) | 364 |
| Third-party review | No |
| Applicant location | Boca Raton, FL, US |

## Why this score
- A long 364-day review suggests additional-information requests: a firm likely to value regulatory help next time.

Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252995). Last refreshed: 2026-11-04T21:30:53.898Z.
Data from the FDA openFDA API, which may lag official FDA databases. Informational only; not regulatory or legal advice.