Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009627506

FEI Number

3009627506

Entity Name

ACCUMOLD LLC

City/State/Country

Ankeny, IA, US

Establishment Address

1711 Se Oralabor Rd, Ankeny, IA 50021, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

AccuMold LLC (Owner Number: 10095628)

Owner / Operator Contact Address

1711 SE Oralabor Road, Ankeny, IA 50021, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PMP	Dorsal Root Ganglion Stimulator For Pain Relief	Unknown	Class 3	N/A	2026-04-06

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AccuMold 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-2367-2024	Abbott Medical	3	Abbott Proclaim DRG Implantable Pulse Generator, REF 3664, Sterile EO, Rx Only

Similar Registrations

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3038429246	EPTAM PRECISION MOLDING MA (A DIVISION OF EPTAM PRECISION)	Lancaster, MA, US
3019807891	CENTERPIECE S. DE R.L DE C.V (sterilization site)	Tijuana Baja California, MX

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009627506. Last updated year: 2026. Please use registration number 3009627506 when referencing this establishment in official correspondence.