SEASIDE MARINE INTERNATIONAL DRUG CO., INC.

FDA Device Registration & Listing · San Pedro, CA, US · Registration 3011767915

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
3011767915
FEI Number
3011767915
Entity Name
SEASIDE MARINE INTERNATIONAL DRUG CO., INC.
City/State/Country
San Pedro, CA, US
Establishment Address
599 W 7TH ST, San Pedro, CA 90731, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Seaside Marine International Drug Co., Inc. (Owner Number: 10049653)
Owner / Operator Contact Address
599 W. 7th St., San Pedro, CA 90731, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

FAK360

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAW Generator, Oxygen, Portable Anesthesiology Class 2 868.5440 2026-01-05
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2026-01-05
OVR Kit, First Aid, Talking General, Plastic Surgery Class 1 878.4014 2026-01-05

Official Correspondent

Matt Seibert

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Seaside Marine International Drug Co., Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K003939 Invacare Corp. VENTURE HOME FILL II, MODEL IOH 200 2001-03-21
K942357 Healthdyne, Inc. H-500 ALLIANCE OXYGEN CONCENTRATOR 1994-05-27
K042262 Sequal Technologies, Inc. INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10 2004-09-10
K003472 Sequal Technologies, Inc. INTEGRA OXYGEN CONCENTRATORS MODEL 6400-OM 2001-06-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0038-2007 Sunrise Medical 2
DeVilbiss iFill Personal Oxygen Station model number 535D.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011767915. Last updated year: 2026. Please use registration number 3011767915 when referencing this establishment in official correspondence.
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