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Sign in to claim this brandARMM INC.
US
Last updated May 27, 2026
What ARMM INC. makes
ARMM Inc. manufactures pleural catheters, non-bioabsorbable closed-wound drains, and mediastinal drainage catheters for fluid management in surgical and post-operative settings. Their portfolio also includes sump drains, single-use endoscopic insufflation tubing sets, and reusable surgical irrigation/aspiration tubing sets, along with connectors for wound drainage systems. The company produces an insufflator filter assembly for laparoscopic procedures and reusable irrigation tubing sets for surgical applications.
ARMM Inc.’s devices are regulated under FDA classifications, including Class I and Class II, with submissions documented through 510(k) clearances and Unique Device Identifiers (UDIs). The products are listed in the FDA’s regulatory databases, ensuring compliance with U.S. medical device requirements. The company operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- armminc.com
- —
- —
- [email protected]
- Phone
- 7148488190
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 797391778
Catalogue (111)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MedDrain | 22204C | FDA UDI | Class I | Active |
| MedDrain | 22207C | FDA UDI | Class I | Active |
| Aspiration Tubing | 51408 | FDA UDI | Class II | Active |
| MedDrain | 242076C | FDA UDI | Class I | Active |
| MedDrain | 242079 | FDA UDI | Class I | Active |
| MedDrain | 23224C | FDA UDI | Class I | Active |
| Insufflator Filter Assembly | 21002 | FDA UDI | Class II | Active |
| Super-Flow Tubing | K922245 | FDA 510(k) | Class II | Active |
| Superflow Irrigation And Aspiration Tubing Sets | K981286 | FDA 510(k) | Class II | Active |
| Endosi Suction Irrigator | K923201 | FDA 510(k) | Class II | Active |
| Meddrains | K931607 | FDA 510(k) | Class I | Active |
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