INNOVATIVE PLASTICS

FDA Device Registration & Listing · Orangeburg, NY, US · Registration 3008278641

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008278641
FEI Number
3008278641
Entity Name
INNOVATIVE PLASTICS
City/State/Country
Orangeburg, NY, US
Establishment Address
400 Route 303, Orangeburg, NY 10962, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Innovative Plastics (Owner Number: 10080206)
Owner / Operator Contact Address
400 Route 303, Orangeburg, NY 10962, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Clearasil Overnight Spot Patches

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2021-06-08

Official Correspondent

Peter Streitman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Innovative 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 3008278641. Last updated year: 2026. Please use registration number 3008278641 when referencing this establishment in official correspondence.
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