Omniguide, Inc.
Omniguide, Inc. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2021, with 1 FDA device recall on record.
Top product codes for Omniguide, Inc.
FDA recalls by Omniguide, Inc.
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 Omniguide, Inc.
- K203241 — OmniGuide BeamPath OTO-U Fiber
- K183199 — TRIO Handpiece
- K180993 — Beacon Advanced CO2 Laser System
- K140378 — FLEXGUIDE ULTRA BEAMPATH ROBOTIC FIBER CONDUIT
- K093451 — OMNIGUIDE BEAMPATH CO2 MARK III WAVEGUIDE FIBER WITH LOW PROFILE/LOW LOSS TIP
- K093251 — OMNIGUIDE BEAMPATH FELS 25A CO2 LASER SYSTEM
- K081939 — OMNIGUIDE BEAMPATH FIBER OPTIC HANDPIECE SYSTEM AND STERILIZATION TRAY
- K073313 — MARK III WAVEGUIDE FIBER WITH LOW PROFILE TIP
- K073409 — OMNIGUIDE STERILE WAVEGUIDE ADAPTER SYSTEM
- K070157 — OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER
- K070071 — OMNIGUIDE ZERO FLOW ZF-T WAVEGUIDE FIBER
- K063141 — OMNIGUIDE ZERO FLOW ZF-T 150 WAVEGUIDE FIBER
- K062423 — OMNIGUIDE BEAMPATH LASER BEAM DELIVERY SYSTEM
- K061909 — HIGHLAND BEAM DELIVERY SYSTEM, MODEL 3-099-002-00-00
Data sourced from openFDA. This site is unofficial and independent of the FDA.