Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014129616

FEI Number

3014129616

Entity Name

ADROIT SURGICAL LLC

City/State/Country

Oklahoma City, OK, US

Establishment Address

10001 Broadway Extension, Suite A, Oklahoma City, OK 73114, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Adroit Surgical LLC (Owner Number: 10055993)

Owner / Operator Contact Address

13904 Quailbrook Drive, Oklahoma City, OK 73134, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tactical Voir Bougie Vie Scope bebe Vie Scope

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCD	Bougie, Esophageal, Ent	Ear, Nose, Throat	Class 1	874.4420	2017-10-25
CCW	Laryngoscope, Rigid	Anesthesiology	Class 1	868.5540	2017-10-25

Official Correspondent

Paul Hagen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Adroit Surgical LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0144-2024	Covidien	1	Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014129616. Last updated year: 2026. Please use registration number 3014129616 when referencing this establishment in official correspondence.