CROWN LABORATORIES, INC.

FDA Device Registration & Listing · Johnson City, TN, US · Registration 3012481754

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
3012481754
FEI Number
1019820
Entity Name
CROWN LABORATORIES, INC.
City/State/Country
Johnson City, TN, US
Establishment Address
349 Lafe Cox Drive, Johnson City, TN 37604, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Crown Laboratories, Inc. (Owner Number: 10051906)
Owner / Operator Contact Address
349 Lafe Cox Drive, Johnson City, TN 37604, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
DEN160029
PMA Number
N/A

All Registered Proprietary Names

Boost 2+ Flex SkinPen Precision Elite SkinPen Precision System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2019-03-19
QAI Powered Microneedle Device General, Plastic Surgery Class 2 878.4430 2024-10-16
QAI Powered Microneedle Device General, Plastic Surgery Class 2 878.4430 2019-03-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Crown Laboratories, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012481754. Last updated year: 2026. Please use registration number 3012481754 when referencing this establishment in official correspondence.
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