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Bicon, LLC

Active in EUDAMED
Also registered as Bicon, Inc.

United Statesfrom SRN EUDAMED FDA SRN US-MF-000002782 FEI 1000305589

Devices
847
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI
Authorised rep.
Bicon Europe LtdIE

What Bicon, LLC makes

BICON, LLC manufactures a range of dental implant and surgical instruments, including permanent pre‑formed implant suprastructures, temporary single‑use suprastructures, one‑piece basket endosteal implants, reusable cannulated drill bits, reusable fixture/appliance drill bits, complete dental implant systems, surgical procedure kits, and reusable instrument trays. Specific device names in the portfolio include the Locator®, Guided Inserter, Guided Spade Drill, Guided Reamer, Brevis, and various implant models.

The company's devices fall under multiple regulatory classes (Class I, II, III, IIa, IIb, and U) and are listed in the European EUDAMED database as well as the U.S. FDA 510(k) and FDA UDI registries. BICON, LLC is based in the United States.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue847

Newest first, rows 1-50 of 847

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  • Locator® 260-250-505

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Lo 260-200-503

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Listed Registry: GUDID Class:I
  • Healing Abutment 260-350-540

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-365-520

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-240-510

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Implant 260-425-318

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Model 260-102-120

    Listed Registry: GUDID Class:I
  • Listed Registry: GUDID Class:I
  • Brevis 260-425-212

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Implant 260-425-112

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-250-920

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Plug 260-101-115

    Withdrawn Registry: GUDID Class:I
  • Stealth Abutment 260-200-241

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-250-540

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Lo 260-250-504

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Guided Reamer 260-960-380

    Listed Registry: GUDID Class:I
  • Lo 260-200-501

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Implant 260-425-328

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-140-510

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Implant 260-425-320

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Model 260-102-115

    Listed Registry: GUDID Class:I
  • Listed Registry: GUDID Class:I
  • Implant 260-425-210

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Guided Reamer 260-935-360

    Listed Registry: GUDID Class:I
  • Model 260-102-501

    Listed Registry: GUDID Class:I
  • Locator® 260-300-503

    Active Regimes: 510(k) Registry: GUDID Class:II
  • 260-028-202

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Healing Abutment 260-150-910

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Locator® 260-250-504

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Implant 260-425-310

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Lo 260-300-503

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-250-211

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Trinia 260-612-120

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Integra-CP 260-345-256

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Integra-Ti 260-160-357

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Locator® 260-200-501

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Integra-CP 260-360-357

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Lo 260-300-501

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-150-510

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Model 260-102-508

    Listed Registry: GUDID Class:I
  • Non-Shouldered Abutment 260-350-350

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Listed Registry: GUDID Class:I
  • Healing Abutment 260-150-920

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-350-920

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Lo 260-300-505

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Healing Abutment 260-240-520

    Active Regimes: 510(k) Registry: GUDID Class:II
  • 260-028-425

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Healing Abutment 260-150-940

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Locator® 260-200-503

    Active Regimes: 510(k) Registry: GUDID Class:II

Rows 1-50 of 847

Showing 1-50 of 847

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000002782
FDA FEI number
1000305589
DUNS number
945015758
EUDAMED status
Active
EUDAMED registered name
Bicon, LLC
Registered address
501 Arborway, 02130, Boston, United States
Website
www.bicon.com
Phone
+16175244443
PRRC contact
Richard Wu(public in EUDAMED)

Frequently asked questions

How many devices does BICON, LLC have in the registry?

The registry currently lists 847 devices for BICON, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list BICON, LLC's devices?

Among its 50 most recently registered devices, BICON, LLC has devices listed in FDA GUDID (50 devices).

What risk classes do BICON, LLC's devices fall under?

Among its 50 most recently registered devices, the classes recorded for BICON, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from BICON, LLC in the registry?

The most recently registered devices listed for BICON, LLC include Locator® 260-250-505, LO 260-200-503, Guided Inserter 260-960-430 and Healing Abutment 260-350-540.

Generated automatically from registry data and not verified by a human reviewer.