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Sign in to claim this brandJessop Precision Products Inc.
US
Last updated May 24, 2026
What Jessop Precision Products Inc. makes
Jessop Precision Products Inc. manufactures single-use and reusable skin marking stickers and guides, including adhesive markers for surgical planning and patient positioning. Their portfolio also includes radiographic image markers for medical imaging alignment and dental guided surgery spatial markers to assist in precision navigation. Additional products feature relief tabs for enhanced adhesion and specialized lines for aesthetic applications.
The company’s devices are classified under FDA Class I, with all products listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in the United States, adhering to regulatory requirements for low-risk medical devices.
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 Jessop Precision Products Inc. manufacture?
Jessop Precision Products Inc. specializes in skin marking devices, including single-use and reusable products like adhesive stickers and guides. Their portfolio includes skin marking stickers for surgical planning and patient positioning, radiographic image markers for aligning medical imaging, and dental guided surgery spatial markers used for precision navigation. Some products also feature relief tabs for better adhesion or specialized lines for aesthetic applications.
Where is Jessop Precision Products Inc. based?
Jessop Precision Products Inc. is based in the United States. The company operates within the US regulatory framework, which governs the design, manufacturing, and distribution of its medical devices.
Which regulatory registries list Jessop Precision Products Inc.’s devices?
Jessop Precision Products Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for medical devices authorized in the United States, particularly for Class I products.
How are Jessop Precision Products Inc.’s devices classified under FDA regulations?
Jessop Precision Products Inc.’s devices fall under FDA Class I classification. This classification applies to low-risk medical devices that pose minimal potential harm to patients, requiring less stringent regulatory oversight compared to higher-risk categories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- suremark.com
- —
- —
- [email protected]
- Phone
- 800-406-3399
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 055127831
Catalogue (63)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Scaneez | Scaneez DentureMark Upper Lateral | FDA UDI | Class I | Active |
| BeautyLine | Clearmark Mole Marker on BeautyLine Butterfly Label | FDA UDI | Class I | Active |
| DentalMark | DentalMark 2.0mm flat fiducial markers | FDA UDI | Class I | Active |
| Clearmarks | Metal Free Semi Lucent Triangle | FDA UDI | Class I | Active |
| ComfortMark | 1.5mm Lead Ball Conformable Nipple Marker ( | FDA UDI | Class I | Active |
| Scaneez | Scaneez DentureMark Universal Molar | FDA UDI | Class I | Active |
| Scaneez | Scaneez DentureMark Universal Bicuspid | FDA UDI | Class I | Active |
| Suremark Left | 1.2cm (0.5 inch) Left "L" Marker on disposable label | FDA UDI | Class I | Active |
| Suremark Relief Tabs | 2.0mm lead ball on relief tabbed label | FDA UDI | Class I | Active |
| Visionline Kids | VisionLine Kids 2.5mm Unicorn | FDA UDI | Class I | Active |
| Visionline Kids | VisionLine Kids 2.5mm Kitten | FDA UDI | Class I | Active |
| Suremark Relief Tabs | 2.5mm lead ball on relief tabbed label | FDA UDI | Class I | Active |
| Clearline | 2.5mm Clearline wire on diamond label | FDA UDI | Class I | Active |
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