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US
Last updated May 23, 2026
What MAXILL, INC. makes
MAXILL, INC. manufactures a range of disposable medical and dental products, including powder‑free nitrile examination gloves, vinyl examination gloves, single‑use sterilization packaging, dental floss varieties, single‑use surgical face masks, reusable eye splash shields, ultrasonic dental scaling handpiece tips, and single‑use dental suction cannulae.
The devices are classified as Class I or Class II medical devices and are listed in the FDA UDI registry. MAXILL, INC. is headquartered 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 MAXILL, INC. manufacture?
MAXILL, INC. manufactures nitrile examination/treatment gloves (non-powdered, non-antimicrobial), vinyl examination/treatment gloves (non-powdered), single-use sterilization packaging, dental floss, single-use surgical/medical face masks, reusable eye splash shields, ultrasonic dental scaling/debridement system handpiece tips, and single-use dental suction system cannulae. These products are designed for use in medical and dental settings and are listed in the FDA UDI registry as Class I or Class II devices.
Where is MAXILL, INC. based?
MAXILL, INC. is headquartered in the United States, as stated in the device data summary. The company’s location is specified under the COUNTRY field as US, confirming its base of operations is within the United States.
In which regulatory registry are MAXILL, INC.'s devices listed?
MAXILL, INC.'s devices are listed in the FDA UDI (Unique Device Identification) registry. This is explicitly stated in the LISTED IN field and confirmed in the SUMMARY, which notes that the devices are classified and listed in the FDA UDI system. The registry tracks device identifiers for traceability and post-market surveillance.
How are MAXILL, INC.'s devices classified under medical device regulations?
MAXILL, INC.'s devices are classified as either Class I or Class II medical devices. This classification is directly provided in the DEVICE CLASSES field and reiterated in the SUMMARY. Class I devices are subject to general controls, while Class II devices require special controls; the company does not manufacture Class III devices based on the provided data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 079343581
Catalogue (544)
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Maxill, Inc. ST. THOMAS Ontario · CA FEI 3005558160