Generica Medical International

FDA Device Registration & Listing · La Verne, CA, US · Registration 3010331226

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
3010331226
FEI Number
3010331226
Entity Name
Generica Medical International
City/State/Country
La Verne, CA, US
Establishment Address
1910 D ST, La Verne, CA 91750, US
Establishment Type(s)
Repack or Relabel Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Generica Medical International (Owner Number: 10044483)
Owner / Operator Contact Address
1920 D ST, La Verne, CA 91750, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K181426
PMA Number
N/A

All Registered Proprietary Names

Generica Medical Enteral Delivery Gravity Bag Set Generica Medical Enteral Delivery Gravity Bag Set with ENFit Generica Medical Cross Spike Plus Generica Medical Enteral Delivery Pump Bag Set with ENFit Generica Medical Cross Spike Plus with ENFit Generica Medical Enteral Delivery Pump Bag Set Generica Medical 60ml Enteral Syringe With Enfit & Transitional Adapter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FPD Tube, Feeding Gastroenterology, Urology Class 2 876.5980 2014-09-12
KNT Tubes, Gastrointestinal (And Accessories) Gastroenterology, Urology Class 2 876.5980 2014-09-12
PNR Enteral Syringes With Enteral Specific Connectors Gastroenterology, Urology Class 2 876.5980 2024-11-26

Official Correspondent

Len Hoffstetter

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Generica Medical International
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
K900590 Biosearch Medical Products, Inc. BIOSEARCH DOBBHOFF(R) GASTROTRAC JEJUNAL FEEDING 1990-08-02
K102548 Footprint Medical, Inc. FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE 2010-11-26
K955248 United States Endoscopy Group, Inc. U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT 1996-05-21
K872921 Medical Support, Inc. MSS ENTERAL DELIVERY SET 1987-12-03
K180622 Covidien Kangaroo Gastrostomy Feeding Tube with ENFit Y-Port 2018-10-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010331226. Last updated year: 2026. Please use registration number 3010331226 when referencing this establishment in official correspondence.
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