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METREX RESEARCH

United States·US-MF-000043710

Last updated September 17, 2026

What METREX RESEARCH makes

Metrex Research manufactures reusable surgical binoculars, including loupes and powered loupes for precision procedures, as well as general-purpose light sources like LED curing lights and headlight systems for surgical illumination. Their portfolio also includes single-use dental polishing cups, non-sterile instrument drapes, and protective covers for cables, leads, sensors, and probes. Additionally, they produce cleaning and disinfection wipes, disinfection agents, and decontamination agents for medical device reprocessing.

The company’s devices are classified under EU Medical Device Regulations as Class I and Class II, with corresponding FDA UDI listings. Their products are registered in the EU’s eudamed database and the FDA’s UDI system, reflecting compliance with regulatory requirements for both reusable and single-use medical instruments. The manufacturer is based in the United States.

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

Information

Country: United States
Address: 28210, Wick Road, Romulus, United States
Website: www.kerrdental.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +18005377123
PRRC Contact: Jennifer Evans
EUDAMED SRN: US-MF-000043710
FDA FEI Number: 1000117344
DUNS Number: —

Catalogue (437)

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Device	Model / Reference	Registries	Class	Status
Orascoptic - OmniOptic HDL 4.5	OmniOptic HDL 4.5	EUDAMEDFDA UDI	Class I	Active
Perfect Pearl	10-9511	FDA UDI	Class I	Active
Orascoptic - Endeavour XL Headlight System	910119-42	FDA UDI	Class I	Active
Orascoptic - Endeavour TruColor XL Headlight System	910131-43	FDA UDI	Class I	Active
HDL™ 3.5 Prism Rx - Dragonfly™	.HDL 3.5.TTL.DRAGONFLY * (GEN 2).*, Rx	FDA UDI	Class I	Active
HDL Ergo 5.0 Plano	HDL Ergo 5.0 Plano	EUDAMEDFDA UDI	Class I	Active
H.P. Sleeve	4050C	EUDAMEDFDA UDI	Class II	Active
XV1™ - Headlight only - plano	.SAFETYGLASSES.XV1.*	FDA UDI	Class I	Active
Orascoptic - Endeavour TruColor Headlight System	910131-4	FDA UDI	Class I	Active
HDL™ 2.5 Macro Rx - XV1™	.HDL 2.5 MACRO.TTL.XV1.*, Rx	FDA UDI	Class I	Active
Orascoptic - Endeavour XL Headlight System	910119-47	FDA UDI	Class I	Active
Orascoptic - Endeavour XL Headlight System	910119-64	FDA UDI	Class I	Active
Pinnacle Tray Sleeve	3300-FC	FDA UDI	Class II	Active
Allrap Protective Barriers	HRCL250C	FDA UDI	Class I	Active
Orascoptic - Endeavour Headlight System	910119-25	FDA UDI	Class I	Active
Endeavour MD	910175-3	FDA UDI	Class I	Active
EyeZoom™ Rx - XV1™	.EYEZOOM.TTL.XV1.*, Rx	FDA UDI	Class I	Active
HDL™ 3.0 Plano - Dragonfly™	.HDL 3.0.TTL.DRAGONFLY * (GEN 2).*, Plano	FDA UDI	Class I	Active
Spark TruColor	910174-32	FDA UDI	Class I	Active
Orascoptic - Endeavour Headlight System	910119-6	FDA UDI	Class I	Active
Orascoptic - Endeavour TruColor XL Headlight System	910131-48	FDA UDI	Class I	Active
MetriClean 2	10-8115	FDA UDI	Class I	Active
MetriZyme	10-4015	FDA UDI	Class I	Active
EmPower Fragrance Free	10-4400	FDA UDI	Class I	Active
Orascoptic - EyeZoom Rx	EyeZoom Rx	EUDAMEDFDA UDI	Class I	Active
Universal Flip - Plano	.UNIVERSAL.FLIP.TITAN.ONE-SIZE.*	FDA UDI	Class I	Active
MetriSPONGE	10-4025	FDA UDI	Class I	Active
Orascoptic - Endeavour XL Headlight System	910119-68	EUDAMEDFDA UDI	Class I	Active
Orascoptic - HDL 4.5 Rx	HDL 4.5 Rx	EUDAMEDFDA UDI	Class I	Active
EyeZoom™ Max Rx - Dragonfly™	.EYEZOOM MAX.TTL.DRAGONFLY * (GEN 2).*, Rx	FDA UDI	Class I	Active
MetriZyme	10-4010	FDA UDI	Class I	Active
Metricide	K930284	FDA 510(k)	Class II	Active
Coldcide-2	K950553	FDA 510(k)	Class I	Active
Metricide Plus 30 Liquid Chemical Germicide	K931592	FDA 510(k)	Class II	Active
Kleenaseptic	K981023	FDA 510(k)	Class I	Active
Metricide 28	K931052	FDA 510(k)	Class II	Active
Coldcide-10	K950516	FDA 510(k)	Class I	Active

Related Companies

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FDA Recalls (3)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Metrex Research has three FDA recall records initiated between 2011-09-20 and 2017-01-20, all of which are marked as terminated. The recalls involved Cavicide with Spring Fresh Fragrance due to reported health reactions, Pinnacle Cure Sleeves with incorrect labeling for light guide compatibility, and CaviWipes Extra Large due to potential contamination during packaging.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Jan 20, 2017	Z-1402-2017	—	terminated	Metrex is recalling the CaviWipes Extra Large because they may have been contaminated during the packaging process.
Feb 6, 2012	Z-2267-2012	—	terminated	Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance because the affected lot of product containing this fragance has caused an increase in reported health reactions in some individuals such as headache, nausea, and respiratory discomfort.
Sep 20, 2011	Z-0444-2013	—	terminated	The firm initiated the recall due to a labeling error. The boxes labeled as Pinnacle Cure Sleeve 4511, which fits 11mm light guides, actually contain Pinnacle Cure Sleeves that fit 7mm or 8mm light guides (part number 4500).