INSTANTRONICS

FDA Device Registration & Listing · Durham, NC, US · Registration 3030263612

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
3030263612
FEI Number
3030263612
Entity Name
INSTANTRONICS
City/State/Country
Durham, NC, US
Establishment Address
200 Meredith Dr., Ste 105, Durham, NC 27713, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
INSTANTRONICS (Owner Number: 10089514)
Owner / Operator Contact Address
200 Meredith Dr., Ste 105, Durham, NC 27713, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SS 69 SS 99 Elite Spectrum Lamprobe

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KCW Epilator, High Frequency, Needle-Type General, Plastic Surgery Class 1 878.5350 2023-12-13

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

INSTANTRONICS
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
K954031 R. A. Fischer Co. Corp. COMPU-BLEND EPILATOR 1996-01-05

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030263612. Last updated year: 2026. Please use registration number 3030263612 when referencing this establishment in official correspondence.
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