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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)

Page 2 of 9

Device	Model / Reference	Registries	Class	Status
Orascoptic - Endeavour Headlight System	910119-8	FDA UDI	Class I	Active
Orascoptic - Endeavour Headlight System	910119-2	FDA UDI	Class I	Active
MetriCide Plus 30	10-3205	FDA UDI	Class II	Active
Pinnacle Cure Sleeve	4511C	FDA UDI	Class II	Active
Orascoptic - Dragonfly HDL 4.5 Rx	Dragonfly HDL 4.5 Rx	EUDAMEDFDA UDI	Class I	Active
Endeavour MD	910176-2	FDA UDI	Class I	Active
PerfectPearl Midnight	10-9518	FDA UDI	Class I	Active
CaviWipes1	13-5224	FDA UDI	Class I	Active
Luxe™ 2.5 Semi-custom loupe	910168-2	FDA UDI	Class I	Active
Dispos-a-Bite	7080	FDA UDI	Class I	Active
Pinn-Point Brushes	8200C	FDA UDI	Class I	Active
EyeZoom™ Mini Plano - Dragonfly™	.EYEZOOMMINI.TTL.DRAGONFLY * (GEN 2).*, Plano	FDA UDI	Class I	Active
Orascoptic - Endeavour Headlight System	910119-22	FDA UDI	Class I	Active
Spree	66600C	FDA UDI	Class I	Active
Endeavour™	922010-1	FDA UDI	N/A	Active
Orascoptic - Endeavour XL Headlight System	910119-45	FDA UDI	Class I	Active
Orascoptic - Spark Headlight System	910118-42	FDA UDI	Class I	Active
Pinnacle X-Ray Sensor Sheaths	PSS3320C	FDA UDI	Class II	Active
Orascoptic - Dragonfly EyeZoom Mini	Dragonfly EyeZoom Mini	FDA UDI	Class I	Active
Pinnacle Cover-All	3700-CC	FDA UDI	Class II	Active
HDL™ 2.5 Micro Plano - Dragonfly™	.HDL 2.5 MICRO.TTL.DRAGONFLY * (GEN 2).*, Plano	FDA UDI	Class I	Active
HDL™ 2.5 Micro Plano - XV1™	.HDL 2.5 MICRO.TTL.XV1.*, Plano	FDA UDI	Class I	Active
PerfectPearl Classic	10-9514	FDA UDI	Class I	Active
Seal-Tight	77500C	FDA UDI	Class I	Active
Orascoptic - Dragonfly HDL 2.5 Macro	Dragonfly HDL 2.5 Macro	EUDAMEDFDA UDI	Class I	Active
Allrap Protective Barriers	HS500C	FDA UDI	Class I	Active
Endeavour™ TruColor™	910177-1	FDA UDI	Class I	Active
EmPower Foam	10-4224	FDA UDI	Class I	Active
PerfectPearl Midnight	10-9522	FDA UDI	Class I	Active
Luxe™ 2.5 Semi-custom loupe	910169-3	FDA UDI	Class I	Active
Orascoptic - Spark Headlight System	910118-11	FDA UDI	Class I	Active
OmniOptic™ Ocular Pair - HDL™ 3.5 Rx	.HDL 3.5.OMNI.OCULAR ONLY.*	EUDAMEDFDA UDI	Class I	Active
Orascoptic - Spark Headlight System	910118-12	FDA UDI	Class I	Active
Envirocide	13-3325	FDA UDI	Class I	Active
PerfectPearl Midnight	10-9523	FDA UDI	Class I	Active
Orascoptic - Endeavour XL Headlight System	910119-67	FDA UDI	Class I	Active
Allrap Protective Barriers	SXRS250C	FDA UDI	Class I	Active
EyeZoom™ Max Plano - Dragonfly™	.EYEZOOM MAX.TTL.DRAGONFLY * (GEN 2).*, Plano	FDA UDI	Class I	Active
Pinnacle X-Ray Sensor Sheaths	PSS3400C	FDA UDI	Class II	Active
Pinnacle X-Ray Sleeve	3900C	EUDAMEDFDA UDI	Class II	Active
HDL™ 5.5 Plano - XV1™	.HDL 5.5.TTL.XV1.*, Plano	FDA UDI	Class I	Active
Ease-in-Shields™	922269-4	FDA UDI	Class I	Active
Luxe™ 2.5 Semi-custom loupe	910168-1	FDA UDI	Class I	Active
Endeavour™ TruColor™ XL	922010-13	FDA UDI	N/A	Active
EmPower	10-4115	FDA UDI	Class I	Unknown
Allrap Protective Barriers	460CC	FDA UDI	Class I	Active
PerfectPearl Classic	10-9512	FDA UDI	Class I	Active
Allrap Protective Barriers	SGHC125C	FDA UDI	Class I	Active
Orascoptic - Dragonfly HDL 4.5	Dragonfly HDL 4.5	EUDAMEDFDA UDI	Class I	Active
Endeavour™ MD	922473-1	FDA UDI	N/A	Active

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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).