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LASER PERIPHERALS LLC.

US

Last updated September 17, 2026

Information

Country
US
Address
13355 10th ave, Plymouth, MN, 55441
Website
—
LinkedIn
—
Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
1221543
DUNS Number
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Catalogue (179)

Page 4 of 4
DeviceModel / ReferenceRegistriesClassStatus
8000205 8000205
FDA UDI
Class IIActive
Db-1000-Pl DB-1000-PL
FDA UDI
Class IIActive
Dc-800b DC-800B
FDA UDI
Class IIActive
Fc-002 Ac FC-002 AC
FDA UDI
Class IIActive
Htb-800-Pl HTB-800-PL
FDA UDI
Class IIActive
Lg-250-Cn LG-250-CN
FDA UDI
Class IIActive
Lg-250-Cnn-Pl LG-250-CNN-PL
FDA UDI
Class IIActive
Db-600r-1-Pl DB-600R-1-PL
FDA UDI
Class IIActive
Hb-272 HB-272
FDA UDI
Class IIActive
Lg-272-Cnn-Pl LG-272-CNN-PL
FDA UDI
Class IIActive
Db-600-Hpt DB-600-HPT
FDA UDI
Class IIActive
Hb-550-Tr HB-550-TR
FDA UDI
Class IIActive
Db-400 DB-400
FDA UDI
Class IIActive
Lg-272-E-Pl LG-272-E-PL
FDA UDI
Class IIActive
Lg-272-Cne-Pl LG-272-CNE-PL
FDA UDI
Class IIActive
Hb-940-Tr HB-940-TR
FDA UDI
Class IIActive
Dc-600b DC-600B
FDA UDI
Class IIActive
Laseguide Cat # Clf-600d & Clf-1000d K901786
FDA 510(k)
Class IIActive
Laser Peripherals Reusable Holmium Fiber K011207
FDA 510(k)
Class IIActive
Scatterfree Lateral Emitting Fiber K992083
FDA 510(k)
Class IIActive
Laser Peripherals, LLC Family of Bare Laser Fibers K170366
FDA 510(k)
Class IIActive
Laser Peripherals Inc. Scatterfree Fiber K961079
FDA 510(k)
Class IIActive
Ls-905 Fiberchoice Adapter System K974229
FDA 510(k)
Class IIActive
Laseguide 600a, 600b, 400a, 400b For Pulmonary Use K880592
FDA 510(k)
Class IIActive
Laseguide 600a, 600b, 400a, 400b For Ob-Gyn Use K880591
FDA 510(k)
Class IIActive
Laser Peripherals Inc. Bare Fiber K961516
FDA 510(k)
Class IIActive
Laseguide 600a, 600b, 400a, And 400b K874680
FDA 510(k)
Class IIActive
Bare Laser Fiber Models Dblf-40, Dblf-60, Dblf-60-1, Dclf-600b, Dslf-60, Dblf-100 K030959
FDA 510(k)
Class IIActive
Laser Peripherals Holmium Bare Fibers K972272
FDA 510(k)
Class IIActive

Related Companies

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Jun 20, 2014Z-2073-2014—terminated

Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling that indicated a sterility expiration date as '2016-16' as opposed to the intended date of '2016-06'.