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Diamatrix

US

Last updated May 27, 2026

What Diamatrix makes

Diamatrix manufactures reusable ophthalmic surgical instruments, including ocular hooks, spatulas, and manipulators for tissue handling, as well as reusable ophthalmic forceps for soft-tissue manipulation. Their portfolio also includes reusable and single-use ophthalmic knives, reusable intraocular scissors, reusable eyelid specula, and reusable corneal markers. Non-illuminating reusable irrigation, infusion, and aspiration cannulas for ophthalmic procedures are also part of their product line.

The company’s devices are classified under FDA’s Class I and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in surgical and diagnostic ophthalmic procedures and adhere to applicable regulatory standards for medical devices in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Diamatrix manufacture?

Diamatrix specializes in reusable ophthalmic surgical instruments. Their product line includes ocular hooks, spatulas, and manipulators for handling tissue during eye surgeries, as well as reusable forceps designed for soft-tissue manipulation. They also produce reusable ophthalmic knives, intraocular scissors, eyelid specula, and corneal markers. Additionally, Diamatrix offers reusable, non-illuminating irrigation, infusion, and aspiration cannulas for ophthalmic procedures. These devices are primarily used in surgical and diagnostic eye care settings.

Where is Diamatrix based, and what does that mean for their regulatory compliance?

Diamatrix is based in the United States, which means their devices must comply with FDA regulations. The company’s products fall under FDA’s Class I and Unclassified (U) categories, indicating they are generally considered low-risk but still subject to regulatory oversight. Being listed in the FDA’s Unique Device Identifier (UDI) database reflects their compliance with U.S. requirements for device identification and traceability.

Which regulatory registries or databases list Diamatrix’s devices?

Diamatrix’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures that each device has a standardized identifier for tracking, reporting, and regulatory purposes. The UDI system helps streamline compliance and transparency for healthcare providers and regulators.

How are Diamatrix’s devices classified under FDA regulations?

Diamatrix’s devices are classified under two FDA categories: Class I and Unclassified (U). Class I devices are typically the lowest risk and often subject to general controls, while Unclassified (U) devices are evaluated individually based on their specific risks. The classification determines the regulatory pathway and oversight required for each product, ensuring they meet safety and performance standards for use in ophthalmic procedures.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
diamatrix.com
LinkedIn
—
Facebook
—
Phone
281-367-8081
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
809555139

Catalogue (558)

Page 11 of 12
DeviceModel / ReferenceRegistriesClassStatus
Diamatrix C433-25
FDA UDI
Class IActive
Diamatrix M74S
FDA UDI
Class IActive
Diamatrix F800S
FDA UDI
Class IActive
ProTekt PG 44850SS
FDA UDI
Class IActive
ProTekt PG 44880MU
FDA UDI
Class IActive
Diamatrix H140-S-S
FDA UDI
Class IActive
Diamatrix Ltd. H485-1-S
FDA UDI
Class IActive
Diamatrix Ltd. CH60
FDA UDI
Class IActive
Diamatrix F016-2.0
FDA UDI
Class IActive
Diamatrix C215-27
FDA UDI
Class IActive
Diamatrix Ltd. IT-.5-C
FDA UDI
Class IActive
Diamatrix W65-14
FDA UDI
Class IActive
ProTekt PG 44535MU
FDA UDI
Class IActive
Diamatrix Ltd. IS-H
FDA UDI
Class IActive
Diamatrix Ltd. N10-CLT
FDA UDI
Class IActive
Diamatrix S001-C
FDA UDI
Class IActive
Diamatrix Ltd. IT-.5-S
FDA UDI
Class IActive
Diamatrix S012-C
FDA UDI
Class IActive
Diamatrix DDPS04
FDA UDI
UActive
Diamatrix N12-S
FDA UDI
Class IActive
Diamatrix Ltd. H573-D
FDA UDI
Class IActive
Diamatrix Ltd. H420-L-S
FDA UDI
Class IActive
Diamatrix C475-26
FDA UDI
Class IActive
ExactEtch 2342K
FDA UDI
Class IActive
Diamatrix Ltd. F040-1.2
FDA UDI
Class IActive
Diamatrix F406-SH
FDA UDI
Class IActive
Diamatrix L07352S
FDA UDI
Class IActive
Diamatrix N04630
FDA UDI
Class IActive
Diamatrix Ltd. F445S.5
FDA UDI
Class IActive
ExactEtch 2205K
FDA UDI
Class IActive
ExactEtch 2162K
FDA UDI
Class IActive
Diamatrix LTD CW1146
FDA UDI
Class IActive
Diamatrix F301S.12
FDA UDI
Class IActive
Diamatrix Ltd. F608T-A
FDA UDI
Class IActive
Diamatrix W28T-14
FDA UDI
Class IActive
Diamatrix Ltd. N05350.75
FDA UDI
Class IActive
ExactEtch 2410K
FDA UDI
Class IActive
Diamatrix DDPS07
FDA UDI
UActive
Diamatrix C551-27
FDA UDI
Class IActive
Inami & Co., Ltd. M-2215L
FDA UDI
Class IActive
Diamatrix 51770
FDA UDI
Class IActive
Diamatrix Ltd. N03872
FDA UDI
Class IActive
Diamatrix H440-S
FDA UDI
Class IActive
Diamatrix C320
FDA UDI
Class IActive
Diamatrix Ltd S502-CR
FDA UDI
Class IActive
ExactEtch 2411K
FDA UDI
Class IActive
ExactEtch 2565K
FDA UDI
Class IActive
ProTekt PG 44350MU
FDA UDI
Class IActive
Dacrios Opthalmic Knives D3522
FDA UDI
Class IActive
ProTekt PG 44650MU
FDA UDI
Class IActive

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