Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2939142

FEI Number

2939142

Entity Name

Bentec Medical OpCo, LLC.

City/State/Country

WOODLAND, CA, US

Establishment Address

1380 E Beamer St, WOODLAND, CA 95776, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Bentec Medical OpCo, LLC. (Owner Number: 2939142)

Owner / Operator Contact Address

1380 East Beamer St., Woodland, CA 95776, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ventral Wall Defect Reduction Silo Bag

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KGY	Bag, Intestine	General, Plastic Surgery	Class 1	878.4100	2018-12-20

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bentec Medical OpCo, LLC.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2939142. Last updated year: 2026. Please use registration number 2939142 when referencing this establishment in official correspondence.