HAVPAK, INC.

FDA Device Registration & Listing · Malvern, PA, US · Registration 2529851

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
2529851
FEI Number
1000136196
Entity Name
HAVPAK, INC.
City/State/Country
Malvern, PA, US
Establishment Address
27-43 Great Valley Pkwy, Malvern, PA 19355, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
HAVPAK, INC. (Owner Number: 9033889)
Owner / Operator Contact Address
27- 43 Great Valley Parkway, --, Malvern, PA 19355, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GLIDE DENTAL FLOSS PRODUCT GLIDE FLOSS Procter & Gamble

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JES Floss, Dental Dental Class 1 872.6390 1998-05-19

Official Correspondent

Rajendra Patel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HAVPAK, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3017125080 Havpak, Inc. West Chester, PA, US
3014387063 Havpak, Inc. Malvern, PA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2529851. Last updated year: 2026. Please use registration number 2529851 when referencing this establishment in official correspondence.
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