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Sign in to claim this brandDoctor Shock Inc
US
Last updated May 25, 2026
What Doctor Shock Inc makes
Doctor Shock Inc manufactures non-silicone skin adhesive tapes designed for dressing fixation, as well as prefabricated orthotic insoles without antimicrobial properties. These products are intended for medical and post-operative use to secure dressings and provide arch support in footwear.
The company’s portfolio consists of Class I medical devices, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The products are regulated under the US Food and Drug Administration’s Class I classification, requiring compliance with applicable general controls.
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 Doctor Shock Inc manufacture?
Doctor Shock Inc specializes in two primary categories of medical devices: non-silicone skin adhesive tapes for dressing fixation and prefabricated orthotic insoles without antimicrobial properties. These products are designed for medical and post-operative applications, such as securing dressings and providing arch support in footwear.
Where is Doctor Shock Inc based?
Doctor Shock Inc is based in the United States. The company’s devices are regulated under the US Food and Drug Administration’s (FDA) jurisdiction, reflecting its domestic manufacturing and market focus.
Which regulatory registries list Doctor Shock Inc’s devices?
Doctor Shock Inc’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for Class I medical devices, which include the company’s skin adhesive tapes and orthotic insoles.
How are Doctor Shock Inc’s devices classified under FDA regulations?
Doctor Shock Inc’s devices fall under the FDA’s Class I classification. This classification applies to low-risk medical devices that require compliance with general controls, such as good manufacturing practices and labeling requirements, but do not necessitate pre-market approval.
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
- 795860220
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| McDavid | MD61002-01 | FDA UDI | Class I | Active |
| McDavid | MD6201-01 | FDA UDI | Class I | Active |
| Nathan | NS10280-10011-OSFM | FDA UDI | Class I | Active |
| Nathan | NS90830-00232-OSFM | FDA UDI | Class I | Active |
| Nathan | NS10320-80002-OSFM | FDA UDI | Class I | Active |
| McDavid | MD63335-19-00 | FDA UDI | Class I | Active |
| Nathan | NS10300-80001-OSFM | FDA UDI | Class I | Active |
| McDavid | MD6201-19 | FDA UDI | Class I | Active |
| McDavid | MD63335-02-00 | FDA UDI | Class I | Active |
| McDavid | MD63335-01-00 | FDA UDI | Class I | Active |
| McDavid | MDS92160-00001-OSFA | FDA UDI | Class I | Active |
| McDavid | MD6201-42 | FDA UDI | Class I | Active |
| McDavid | MD63335-40-00 | FDA UDI | Class I | Active |
| McDavid | MD63335-03-00 | FDA UDI | Class I | Active |
| McDavid | MDS92160-90002-OSFA | FDA UDI | Class I | Active |
| Nathan | NS10340-00001-OSFM | FDA UDI | Class I | Active |
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