Is this your brand? Sign in to claim ownership.
Sign in to claim this brandDermapac Inc.
US
Last updated May 27, 2026
What Dermapac Inc. makes
Dermapac Inc. manufactures radiopaque woven surgical sponges, general-purpose surgical sponges, and general surgical procedure kits that are non-medicated and single-use. The company also produces general-purpose absorbent tip applicators or swabs, dental and maxillofacial surgical procedure kits (non-medicated, single-use), instrument management bags, surgical soft-tissue manipulation forceps resembling tweezers (single-use), and umbilical cord tape.
All devices manufactured by Dermapac Inc. are classified as Class I medical devices and are listed in the FDA's Unique Device Identification (FDA UDI) system. The company is based in the United States-based.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Dermapac Inc. make?
Dermapac Inc. manufactures radiopaque woven surgical sponges, general-purpose surgical sponges, general surgical procedure kits (non-medicated, single-use), general-purpose absorbent tip applicators or swabs, dental and maxillofacial surgical procedure kits (non-medicated, single-use), instrument management bags, surgical soft-tissue manipulation forceps resembling tweezers (single-use), and umbilical cord tape.
Where is Dermapac Inc. based?
Dermapac Inc. is based in the United States, as indicated by the country field in the device data.
Which registries list Dermapac Inc.'s devices?
Dermapac Inc.'s devices are listed in the FDA's Unique Device Identification (FDA UDI) system, as specified in the LISTED IN field of the device data.
How are Dermapac Inc.'s devices classified?
All devices manufactured by Dermapac Inc. are classified as Class I medical devices, as stated in the DEVICE CLASSES field of the provided data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- [email protected]
- Phone
- 203-924-7148
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 796088466
Catalogue (178)
Page 4 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dermapac, Inc. | 5136 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 6713 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 9991 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 6028 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 6002 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 9003 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 2087 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 5206 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 9962 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 9976 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 5252 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 8811 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 8226 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 9989 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 8122 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 9960 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 5052 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 8692 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 6777 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 8034 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 2142 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 6716 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 9990 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 5054 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 5205 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 7005 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 5040 | FDA UDI | Class I | Active |
| Dermapac, Inc. | 6006 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.