Skip to content

Cambridge Interventional LLC

Active in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000021911 FEI 3015257340

Cambridge Interventional LLC is a medical device manufacturer based in the United States, with 710 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II; EU Class IIb and IIa) as of 13 Nov 2026.

Devices
710
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 573
  • EUDAMED 301
  • FDA 510(k) 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 409
  • EU Class IIb 300
  • EU Class IIa 1
Sites and related companies
Identifiers
  • EUDAMED SRN US-MF-000021911
  • FDA FEI 3015257340
  • DUNS 080897872

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI
Authorised rep.
MDSS GmbHDE

Catalogue710

Newest first, rows 1-50 of 710

Search and filter all 710 devices
Skip device list
  • ProcedureKitCRF CRF-U2035-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-U1535-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1010-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1015-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1007-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1020-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1025-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1035-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1030-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1040-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1045-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1520-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1525-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1510-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1050-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1535-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1507-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1530-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1515-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1540-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1545-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2007-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C1550-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2010-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2015-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2020-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2025-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2030-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2040-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2035-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2045-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2050-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2507-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2510-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2515-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2520-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2525-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2530-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2535-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2545-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2540-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-C2550-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-N1005-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-N1025-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-N1010-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-N1030-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-N1020-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-N1015-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-N1035-K

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ProcedureKitCRF CRF-N1040-K

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

Rows 1-50 of 710

Showing 1-50 of 710

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000021911
FDA FEI number
3015257340
DUNS number
080897872
EUDAMED status
Active
EUDAMED registered name
Cambridge Interventional LLC
Registered address
78, Cambridge Street, 01803, Burlington, United States
Phone
+1 781 221 5300
PRRC contact
Michael Arnold(public in EUDAMED)

From the company website

Read 18 Sep 2026

Cambridge Interventional is a U.S.-based medical device company specializing in radiofrequency ablation (RFA) technology for benign thyroid nodules and other ablations, with FDA-cleared CRF systems featuring audio/visual guidance.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Cambridge Interventional LLC have in the registry?

The registry currently lists 710 devices for Cambridge Interventional LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cambridge Interventional LLC's devices?

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

What risk classes do Cambridge Interventional LLC's devices fall under?

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

What are the newest devices from Cambridge Interventional LLC in the registry?

The most recently registered devices listed for Cambridge Interventional LLC include ProcedureKitCRF CRF-U2035-K, ProcedureKitCRF CRF-U1535-K, ProcedureKitCRF CRF-C1010-K and ProcedureKitCRF CRF-C1015-K.

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