Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012990641

FEI Number

3012990641

Entity Name

ARMOR DENTAL CORP

City/State/Country

Hingham, MA, US

Establishment Address

20 CAMELOT DR, Hingham, MA 02043, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Armor Dental Corporation (Owner Number: 10052711)

Owner / Operator Contact Address

20 Camelot Drive, Hingham, MA 02043, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TissuePro Single Sleeve, MN Retractor Scan-Mate® (Blue) TissuePro Distal Sleeve, MN Retractor Single-Use Scan-Mate® (Black) Scan-Mate® MegaGen TissuePro Distal Sleeve, MN Retractor TissuePro Proximal Sleeve, MN Retractor MirroSoft No. 4 Mirror MirroSoft No. 5 Mirror MirroSoft No. 5 Double Mirror MirroSoft TearDrop Mirror MirroSoft Delta Mirror

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EIF	Accessories, Retractor, Dental	Dental	Class 1	872.4565	2019-02-09
EAX	Mirror, Mouth	Dental	Class 1	872.4565	2025-05-05

Official Correspondent

Cherie Le Penske

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Armor Dental Corporation

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 3012990641. Last updated year: 2026. Please use registration number 3012990641 when referencing this establishment in official correspondence.