Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014351477

FEI Number

3014351477

Entity Name

STIEHL TECH

City/State/Country

Lisle, IL, US

Establishment Address

815 Ogden Avenue, Lisle, IL 60532, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Stiehl Tech, LLC (Owner Number: 10062431)

Owner / Operator Contact Address

111 East Main Street, Salem, IL 62881, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PERILAV Wound Irrigation Kit PERILAV Peristaltic Jet Lavage Irrigator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FON	Bag, Drainage, With Adhesive, Ostomy	Gastroenterology, Urology	Class 1	876.5900	2020-01-25
FQH	Lavage, Jet	General Hospital	Class 2	880.5475	2020-01-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Stiehl Tech, 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
K213616	Becton, Dickinson and Company	BD Surgiphor Antimicrobial Irrigation System	2022-03-23

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3005621808	ANJI HONGDE MEDICAL PRODUCTS CO., LTD.	HUZHOU Zhejiang, CN
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014351477. Last updated year: 2026. Please use registration number 3014351477 when referencing this establishment in official correspondence.