Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017482348

FEI Number

3017482348

Entity Name

QTD PLASTICS

City/State/Country

Meadville, PA, US

Establishment Address

21398 Blooming Valley Road, Meadville, PA 16335, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

QTD Plastics (Owner Number: 10077976)

Owner / Operator Contact Address

21398 Blooming Valley Road, Meadville, PA 16335, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

None None

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2020-10-14
KYG	Device, Irrigation, Ocular Surgery	Ophthalmic	Class 1	886.4360	2020-10-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

QTD Plastics

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 3017482348. Last updated year: 2026. Please use registration number 3017482348 when referencing this establishment in official correspondence.