SOLMETEX, LLC

FDA Device Registration & Listing · Northborough, MA, US · Registration 3003040760

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
3003040760
FEI Number
3003040760
Entity Name
SOLMETEX, LLC
City/State/Country
Northborough, MA, US
Establishment Address
30 Bearfoot Rd., Suite 2, Northborough, MA 01532, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Solmetex, LLC (Owner Number: 10085904)
Owner / Operator Contact Address
50 Bearfoot Rd., Suite 2, Northborough, MA 01532, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DryShield Instrument, dental hand

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DYN Mouthpiece, Saliva Ejector Dental Class 1 872.6640 2022-09-02
DZN Instruments, Dental Hand Dental Class 1 872.4565 2022-09-02

Official Correspondent

Roger Kampf

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Solmetex, LLC
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
K781592 Henry Schein, Inc. SURGICAL ASPIRATOR TIPS 1978-12-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003040760. Last updated year: 2026. Please use registration number 3003040760 when referencing this establishment in official correspondence.
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