Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004915909

FEI Number

3004915909

Entity Name

DRMR LLC

City/State/Country

Centerville, OH, US

Establishment Address

9530 Cutlers Trace, Centerville, OH 45458, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DRMR LLC (Owner Number: 10023547)

Owner / Operator Contact Address

9530 Cutlers Trace, Dayton, OH 45458, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Trocar

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDC	Instrument, Surgical, Disposable	General, Plastic Surgery	Class 1	878.4800	2007-11-30

Official Correspondent

Robert Garbrick

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DRMR LLC

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K831798	I M, Inc.	DISPOSABLE SCALPELS	1983-07-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004915909. Last updated year: 2026. Please use registration number 3004915909 when referencing this establishment in official correspondence.