J. KNIPPER AND COMPANY, INC.

FDA Device Registration & Listing · LAKEWOOD, NJ, US · Registration 2246553

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
2246553
FEI Number
2246553
Entity Name
J. KNIPPER AND COMPANY, INC.
City/State/Country
LAKEWOOD, NJ, US
Establishment Address
ONE HEALTHCARE WAY, LAKEWOOD, NJ 08701, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
J. KNIPPER AND COMPANY, INC. (Owner Number: 9053305)
Owner / Operator Contact Address
ONE HEALTHCARE WAY, --, Lakewood, NJ 08701, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K063860
PMA Number
N/A

All Registered Proprietary Names

Thrombi-Gel

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QSX Hemostatic Wound Dressing With Thrombin Or Other Biologics Unknown Class U N/A 2008-03-28

Official Correspondent

Dominique Bourdeau-Oscar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

J. KNIPPER AND COMPANY, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Other Registrations for Same Entity

Registration Number Establishment Name Location
3014680791 J. Knipper and Company, Inc. Charlestown, IN, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2246553. Last updated year: 2026. Please use registration number 2246553 when referencing this establishment in official correspondence.
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