CARAN PRECISION ENGINEERING & MANUFACTURING CORP.

FDA Device Registration & Listing · Brea, CA, US · Registration 3032760064

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
3032760064
FEI Number
3032760064
Entity Name
CARAN PRECISION ENGINEERING & MANUFACTURING CORP.
City/State/Country
Brea, CA, US
Establishment Address
2830 Orbiter St, Brea, CA 92821, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Caran Precision Engineering & Manufacturing Corp. (Owner Number: 10092006)
Owner / Operator Contact Address
2830 Orbiter Street, Brea, CA 92821, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Super Brush Super Brush

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KXG Applicator, Absorbent Tipped, Sterile General Hospital Class 1 880.6025 2024-11-25
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2024-11-25

Official Correspondent

Melinda Hua

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Caran Precision Engineering & Manufacturing Corp.
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 3032760064. Last updated year: 2026. Please use registration number 3032760064 when referencing this establishment in official correspondence.
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