BioGeniv, INC

FDA Device Registration & Listing · Lenoir, NC, US · Registration 1055876

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
1055876
FEI Number
1000111217
Entity Name
BioGeniv, INC
City/State/Country
Lenoir, NC, US
Establishment Address
640 Nu Way Circle NE, Lenoir, NC 28645, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
BioGeniv, Inc. (Owner Number: 9005582)
Owner / Operator Contact Address
640 NuWay Circle NE, 4457 Hwy 105 S, Lenoir, NC 28645, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Greer Well Greer Picks Greer Pick

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SCL Allergen And Vaccine Delivery Needles General Hospital Class 2 880.5570 2007-12-20
SCL Allergen And Vaccine Delivery Needles General Hospital Class 2 880.5570 2007-12-20

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BioGeniv, 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
K000299 Biomedex, Inc. DERMAPIK II SKIN TEST SYSTEM, DERMAPIK II (SINGLE TEST DEVICE), POLYPIK II (MULTIPLE SKIN TEST DEVICE), DERMAPIK TRAY, D 2000-04-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1055876. Last updated year: 2026. Please use registration number 1055876 when referencing this establishment in official correspondence.
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