ARCULANT, INC.

FDA Device Registration & Listing · Santa Clara, CA, US · Registration 3016544015

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
3016544015
FEI Number
3016544015
Entity Name
ARCULANT, INC.
City/State/Country
Santa Clara, CA, US
Establishment Address
430 Aldo Avenue, Santa Clara, CA 95054, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Arculant, Inc. (Owner Number: 10062280)
Owner / Operator Contact Address
430 Aldo Avenue, Santa Clara, CA 95054, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ARC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTD Forceps General, Plastic Surgery Class 1 878.4800 2020-01-07

Official Correspondent

Moon Pak

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Arculant, 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
K852723 The Huxley Instrument Corp. FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420 1985-07-15
K873512 Arthropedics, Inc. SERRATED GRASPING FORCEPS, RIGHT 1987-11-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016544015. Last updated year: 2026. Please use registration number 3016544015 when referencing this establishment in official correspondence.
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