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Eagle Labs, LLC

Active in EUDAMED
Also registered as Eagle Labs

United Statesfrom SRN EUDAMED FDA SRN US-MF-000011740 FEI 2027619

Eagle Labs, LLC is a medical device manufacturer based in the United States, with 27 devices listed in FDA GUDID and EUDAMED (FDA Class II; EU Class IIa) as of 12 Nov 2026.

Devices
27
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 20
  • EUDAMED 7

A device listed in two registries counts in both.

Device classes
  • FDA Class II 20
  • EU Class IIa 7
Top EMDN categories
Identifiers
  • EUDAMED SRN US-MF-000011740
  • FDA FEI 2027619

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

Catalogue27

Newest first, rows 1-27 of 27

Search and filter all 27 devices
Skip device list
  • Peribulbar Atkinson Tip Ref 102-25-22

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Retrobulbar Atkinson Tip Ref 101-25

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Tri-Port Sub-Tenon Ref 100-19

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Tri-Port Sub-Tenon Ref 100-21C

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Peribulbar Atkinson Tip Ref 102-25-32

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Retrobulbar Atkinson Tip Ref 101-23

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Tri-Port Sub-Tenon Ref 100-19C

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • 810-30

    Listed Registry: GUDID Class:II
  • 620-08

    Listed Registry: GUDID Class:II
  • 810-64

    Listed Registry: GUDID Class:II
  • 600-40

    Listed Registry: GUDID Class:II
  • 810-60

    Listed Registry: GUDID Class:II
  • 620-09

    Listed Registry: GUDID Class:II
  • 600-15

    Listed Registry: GUDID Class:II
  • 620-10

    Listed Registry: GUDID Class:II
  • 600-10

    Listed Registry: GUDID Class:II
  • 600-30

    Listed Registry: GUDID Class:II
  • 500-01

    Listed Registry: GUDID Class:II
  • 600-20

    Listed Registry: GUDID Class:II
  • 810-20

    Listed Registry: GUDID Class:II
  • 500-05

    Listed Registry: GUDID Class:II
  • 810-61

    Listed Registry: GUDID Class:II
  • 810-54

    Listed Registry: GUDID Class:II
  • 810-21

    Listed Registry: GUDID Class:II
  • 600-11

    Listed Registry: GUDID Class:II
  • 600-08

    Listed Registry: GUDID Class:II
  • 810-22

    Listed Registry: GUDID Class:II

Rows 1-27 of 27

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000011740
FDA FEI number
2027619
EU VAT number
FR-08799255393
EUDAMED status
Active
EUDAMED registered name
Eagle Labs, LLC
EUDAMED abbreviated name
Eagle Labs
Registered address
815, Vikings Parkway, 55121, St. Paul, United States
Phone
+001 (651) 789-3966
PRRC contact
Ajay Boodhun(public in EUDAMED)

From the company website

Read 18 Oct 2026

At Eagle Labs guarantee that our products are manufactured with the highest quality standards in the USA. Transforming the way patients and surgeons work and live worldwide.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Eagle Labs, LLC have in the registry?

The registry currently lists 27 devices for Eagle Labs, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Eagle Labs, LLC's devices?

Among its 27 most recently registered devices, Eagle Labs, LLC has devices listed in EUDAMED (7 devices) and FDA GUDID (20 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 27 most recently registered devices, the classes recorded for Eagle Labs, LLC's devices are Class IIa and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Eagle Labs, LLC in the registry?

The most recently registered devices listed for Eagle Labs, LLC include Peribulbar Atkinson Tip, Retrobulbar Atkinson Tip, Tri-Port Sub-Tenon and 810-30.

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