← Back to catalogue

Hard Splint & Thermo-Adaptive Splint

FDA 510(k)

U (US FDA 510(k))

510(k) K241729

by Whip-Mix Corporation

Identifiers

510(k) Number
K241729 FDA 510(k)
FDA Product Code
MQC FDA 510(k)

Classification

Device Class
U FDA 510(k)
Advisory Committee
Unknown FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Hard Splint & Thermo-Adaptive Splint by Whip-Mix Corporation — U — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

FDA Applicant
Whip Mix Corporation

Sources (1)

  • FDA 510(k) K241729 24 fields · synced Jun 18, 2026