W&H Dentalwerk Buermoos GmbH
W&H Dentalwerk Buermoos GmbH holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2026, with 1 FDA device recall on record.
Top product codes for W&H Dentalwerk Buermoos GmbH
FDA recalls by W&H Dentalwerk Buermoos GmbH
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by W&H Dentalwerk Buermoos GmbH
- K253776 — Implantmed Plus II & Piezomed Plus II Module
- K243280 — Piezomed Pro (Piezomed Pro module M-PM100 incl. handpiece M-PH350, Piezomed Pro instruments (various tips) and accessories)
- K201703 — PROXEO Twist Cordless Polishing System PL-40 H
- K181858 — Electric Handpiece Motor
- K171553 — W&H Assistina Twin
- K143704 — Advanced Air System
- K133488 — PIEZOMED
- K100600 — PROSTHODONTIC SCREWDRIVER , MODEL IA-400
- K083811 — W&H HANDPIECE ANESTO, MODEL: RA-5
- K090931 — CORDLESS ENDO HANDPIECES EB-300, ENTRAN AND EB-300 S, S5 ENDO MOTOR
- K090548 — CONTRA-ANGLE HANDPIECE KOMET OS30
- K080939 — SURGICAL HANDPIECES, MIKRO SAW HANDPIECES
- K060287 — DRILLTECH, ISM, IMPLANTUNIT, ZIMMER SURGICAL MOTOR SYSTEM
- K052741 — IMPLANTMED SI-915 (115V VERSION); IMPLANTMED SI-923 (230V VERSION) INCL. ACCESSORIES
- K014068 — ELCOMED, MODELS SA-200 C 230, SA-200 230, SA-200 C 115, SA-200 115
- K011061 — SURGICAL CONTRA-ANGEL HANDPIECES TYPES WS-56E,WS-75E/KM,WS-92 E/3,SURGICAL STRAIGHT HANDPIECES TYPES, S-9, S-10, S-11
- K002469 — IMPLANTMED SI-95 115 (100-130 V) AND SI-95 230 (220-240 V)
- K984508 — SURGICAL CONTRA-ANGLE HANDPIECES, MODELS 975 AE,979 E/KM, 985 AE, 986 AE, 988 E/KM AND SURGICAL STRAIGHT HANDPIECES MOD
Data sourced from openFDA. This site is unofficial and independent of the FDA.