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Sign in to claim this brandFIRST AID BANDAGE CO INC
US
Last updated May 24, 2026
What FIRST AID BANDAGE CO INC makes
The company manufactures sterile surgical and medical sponges, including neurosurgical, ophthalmic, and general-purpose varieties, as well as non-woven and woven gauze pads. It also produces intranasal and ear wicks made from non-biodegradable materials, alongside dissection sponges and non-antimicrobial gauze pads for wound care and surgical applications.
These products are regulated under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identification (UDI) database. The manufacturer operates from 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 FIRST AID BANDAGE CO INC manufacture?
FIRST AID BANDAGE CO INC specializes in sterile surgical and medical sponges, including neurosurgical, ophthalmic, and general-purpose types. Their product line also includes non-woven and woven gauze pads, intranasal splints (non-biodegradable), ear wicks (non-biodegradable), and dissection sponges. These devices are designed for surgical applications, wound care, and medical procedures.
Where is FIRST AID BANDAGE CO INC based?
The company is headquartered in the United States. This location influences its regulatory compliance, as its devices are subject to FDA oversight under U.S. medical device regulations.
Which regulatory registries list devices manufactured by FIRST AID BANDAGE CO INC?
The company’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability in the healthcare supply chain.
How are devices from FIRST AID BANDAGE CO INC classified under FDA regulations?
The company’s products fall under FDA’s Class I, Class II, and Unclassified (U) categories. Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve special controls to ensure safety and effectiveness. Unclassified devices are still subject to FDA review but may not fit neatly into the standard risk-based classifications.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- fabco.net
- —
- —
- [email protected]
- Phone
- 8604438499
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 001137280
Catalogue (115)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Fabco | 34824010 | FDA UDI | Class I | Active |
| Fabco | 34633010 | FDA UDI | Class I | Active |
| Fabco | 35504410 | FDA UDI | U | Active |
| Fabco | 35523810 | FDA UDI | U | Active |
| Fabco | 35501110 | FDA UDI | U | Active |
| Fabco | 34861010 | FDA UDI | Class I | Active |
| Fabco | 37000010 | FDA UDI | Class I | Active |
| Fabco | 35529810 | FDA UDI | U | Active |
| Fabco | 34340810 | FDA UDI | Class I | Active |
| Fabco | 34103010 | FDA UDI | Class I | Active |
| Fabco | 37002010 | FDA UDI | Class I | Active |
| Fabco | 35520810 | FDA UDI | U | Active |
| Fabco | 35500410 | FDA UDI | U | Active |
| Fabco | Q604200 | FDA UDI | Class II | Active |
| Fabco | Q605203 | FDA UDI | Class I | Active |
| Fabco | Q604205 | FDA UDI | Class II | Active |
| Fabco | Q604007 | FDA UDI | Class II | Active |
| Fabco | 35503610 | FDA UDI | U | Active |
| Fabco | 34831010 | FDA UDI | Class I | Active |
| Fabco | 34865010 | FDA UDI | Class I | Active |
| Fabco | 31101010 | FDA UDI | Class I | Active |
| Fabco | 34860210 | FDA UDI | Class I | Active |
| Fabco | 34770510 | FDA UDI | Class I | Active |
| Fabco | Q600320 | FDA UDI | Class I | Active |
| Fabco | Q604230 | FDA UDI | Class II | Active |
| Fabco | Q770409 | FDA UDI | Class I | Active |
| Fabco | 35502210 | FDA UDI | U | Active |
| Fabco | Q605202 | FDA UDI | Class I | Active |
| Fabco | 34821511 | FDA UDI | Class I | Active |
| Fabco | 35500610 | FDA UDI | U | Active |
| Fabco | 35503310 | FDA UDI | U | Active |
| Fabco | 34440210 | FDA UDI | Class I | Active |
| Fabco | 34880210 | FDA UDI | Class I | Active |
| Fabco | 34723010 | FDA UDI | Class I | Active |
| Fabco | 34322210 | FDA UDI | Class I | Active |
| Fabco | Q770319 | FDA UDI | Class I | Active |
| Fabco | 35501610 | FDA UDI | U | Active |
| Fabco | 35501310 | FDA UDI | U | Active |
| Fabco | Q604204 | FDA UDI | Class II | Active |
| Fabco | 34901510 | FDA UDI | Class I | Active |
| Fabco | 37001010 | FDA UDI | Class I | Active |
| Fabco | 34106010 | FDA UDI | Class I | Active |
| Fabco | Q604250 | FDA UDI | Class II | Active |
| Fabco | 34116010 | FDA UDI | Class I | Active |
| Fabco | Q770411 | FDA UDI | Class I | Active |
| Fabco | 34102010 | FDA UDI | Class I | Active |
| Fabco | 34771010 | FDA UDI | Class I | Active |
| Fabco | 36171111 | FDA UDI | Class I | Active |
| Fabco | 34138111 | FDA UDI | Class I | Active |
| Fabco | 34320510 | FDA UDI | Class I | Active |
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