510(k) K243280

Device
Piezomed Pro (Piezomed Pro module M-PM100 incl. handpiece M-PH350, Piezomed Pro instruments (various tips) and accessories)
Applicant
W&H Dentalwerk Buermoos GmbH
510(k) number
K243280
Product code
ERL
Decision
Substantially Equivalent (SESE)
Decision date
2025-07-03
Date received
2024-10-17
Regulation
874.4250
Classification name
Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
Medical specialty
Ear, Nose, Throat
Review panel
Ear, Nose, Throat
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Gerhard Weidler
Address
Ignaz-Glaser-Straße 53 Buermoos AT 5111 5111

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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