Data / Medical devices / United States / Hood Container Corporation

Hood Container Corporation: FDA-registered device maker in Rural Hall, NC, United States, 3 510(k) clearances and 1 PMA approval

Name: Hood Container Corporation FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Hood Container Corporation is registered with the FDA (registration 1067084) in Rural Hall, NC, United States. It lists 6 device types. The FDA files 3 510(k) clearances and 1 PMA approval under its listings, the newest dated November 1, 2006. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 1067084
FEI number: 3003495738
Address: 300 Forum Pkwy --, Rural Hall, NC, United States, 27045
Owner or operator: Hood Container Corporation (9048058)
Roles: Repackager or relabeler
First device listed: October 9, 2001
Registered through: 2027
Brand names listed: Hood Container, Johnson & Johnson Vision Care, Vicks ZzzQuil Sleep Nasal Strips Ultra

Devices it lists

Device	Product code	Class	Role	Source
Dilator, Nasal	LWF	1	Repackager or relabeler	accessdata.fda.gov
Lens, Contact, (Disposable)	MVN	2	Repackager or relabeler	accessdata.fda.gov
Lenses, Soft Contact, Daily Wear	LPL	2	Repackager or relabeler	accessdata.fda.gov
Lenses, Soft Contact, Extended Wear	LPM	3	Repackager or relabeler	accessdata.fda.gov
Toothbrush, Manual	EFW	1	Repackager or relabeler	accessdata.fda.gov
Toothbrush, Powered	JEQ	1	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
November 1, 2006	K062614	VISTAKON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS, CLEAR AND TINTED (VISIBILITY AND/OR COSMETICALLY)	LPL	Substantially Equivalent	Johnson & Johnson Vision Care, Inc.	accessdata.fda.gov
August 12, 2005	K051900	ACUVUE (ETAFILCON A) CONTACT LENS, CLEAR AND WITH VISIBILITY TINT WITH UV BLOCKER, FOR DAILY WEAR	MVN	Substantially Equivalent	Johnson & Johnson Vision Care, Inc.	accessdata.fda.gov
October 16, 2003	K032340	VISTAKON (GALYFILCON A) SOFT CONTACT LENS	LPL	Substantially Equivalent	Johnson & Johnson Vision Care, Inc.	accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Approved	PMA number	Device	Product code	Supplements	Latest decision	Source
March 18, 1980	N18033	ACUVUE CONTACT LENS	LPM	107	April 17, 2026	accessdata.fda.gov

Compare with other makers

Updated April 17, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.