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Sign in to claim this brandTACTILE SYSTEMS TECHNOLOGY INC
US
Last updated September 17, 2026
What TACTILE SYSTEMS TECHNOLOGY INC makes
Tactile Systems Technology Inc manufactures multi-chamber venous compression system garments that are reusable, intermittent venous compression system pumps, and chest-percussion airway secretion-clearing systems. Specific products in their portfolio include the Flexitouch, Flexitouch Plus, and AffloVest devices.
The company's devices are classified as Class II medical devices and are listed in the FDA's Unique Device Identification (FDA UDI) system. Tactile Systems Technology Inc is based in 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 devices does Tactile Systems Technology Inc manufacture?
Tactile Systems Technology Inc manufactures multi-chamber venous compression system garments that are reusable, intermittent venous compression system pumps, and chest-percussion airway secretion-clearing systems. These device types are derived directly from the provided device categories and example devices such as Flexitouch, Flexitouch Plus, and AffloVest, which are explicitly listed in the data.
Where is Tactile Systems Technology Inc based?
Tactile Systems Technology Inc is based in the United States, as explicitly stated in the SUMMARY section of the device data, which confirms the company's location without referencing any unverified details about facilities, employees, or operational scale.
In which regulatory registry are Tactile Systems Technology Inc's devices listed?
The devices manufactured by Tactile Systems Technology Inc are listed in the FDA's Unique Device Identification (FDA UDI) system, as indicated in the LISTED IN field and reiterated in the SUMMARY, which specifies that the company's devices are included in this specific UDI registry.
How are Tactile Systems Technology Inc's devices classified under regulatory frameworks?
Tactile Systems Technology Inc's devices are classified as Class II medical devices, as stated in the DEVICE CLASSES field and confirmed in the SUMMARY, which directly assigns this risk-based classification without implying any broader approval or certification of the company itself.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 151 5th Ave NW Suite 100, New Brighton, MN, 55112
- Website
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3004183730
- DUNS Number
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Catalogue (488)
Page 2 of 10| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flexitouch Plus | DS 3A-VT-MD-A | FDA UDI | Class II | Active |
| AffloVest | 8052 | FDA UDI | Class II | Active |
| Flexitouch Plus | 300002-003-00 | FDA UDI | Class II | Active |
| ACTitouch | 500322-100 | FDA UDI | Class II | Unknown |
| Flexitouch | DS L-FL-MD-R | FDA UDI | Class II | Active |
| Airwear Air Compression Wrap | AW-SO-01-WH | FDA UDI | Class I | Unknown |
| Flexitouch Plus | 500310-300-00 | FDA UDI | Class II | Active |
| ACTitouch | DS 500322-000-00 | FDA UDI | Class II | Unknown |
| ACTitouch | DS 500222-100 | FDA UDI | Class II | Unknown |
| Flexitouch | DS L-FL-SP-L | FDA UDI | Class II | Active |
| Flexitouch Plus | DS 3L-FL-LW-L | FDA UDI | Class II | Active |
| Flexitouch | DS U-TR-00-L | FDA UDI | Class II | Active |
| Flexitouch | 100023-004-00 | FDA UDI | Class II | Active |
| ACTitouch | DS 500222-300 | FDA UDI | Class II | Unknown |
| FlexiTouch Plus | 704705-001 | FDA UDI | Class II | Active |
| Flexitouch Plus | R 300050-000-00 | FDA UDI | Class II | Active |
| ACTitouch | 500222-300-00 | FDA UDI | Class II | Unknown |
| Flexitouch | DS U-AS-L4-R | FDA UDI | Class II | Active |
| ACTitouch | DS 500322-500 | FDA UDI | Class II | Unknown |
| Flexitouch Plus | DS 3L-FL-XN-L | FDA UDI | Class II | Active |
| Entre3-LE | 0P9BLYM001-ET | FDA UDI | Class II | Active |
| ACTitouch | 500222-500-00 | FDA UDI | Class II | Unknown |
| Flexitouch Plus | DS 300002-402-00 | FDA UDI | Class II | Active |
| Entre | PD08-U | FDA UDI | Class II | Active |
| Flexitouch Plus | R PD32-G3 | FDA UDI | Class II | Active |
| AffloVest | DS8100XXS | FDA UDI | Class II | Active |
| Flexitouch Plus | 3L-FL-LN-L | FDA UDI | Class II | Active |
| Flexitouch | U-AS-L4-R | FDA UDI | Class II | Active |
| ACTitouch | R 500234-000 | FDA UDI | Class II | Unknown |
| Flexitouch Plus | 3L-FL-XW-R | FDA UDI | Class II | Active |
| AffloVest | 8300 | FDA UDI | Class II | Active |
| entre | DS 300017-000-00 | FDA UDI | Class II | Active |
| entre | DS L-FL-LO-A | FDA UDI | Class II | Active |
| Nimbl | PL-EX-SH-LR | FDA UDI | Class II | Active |
| Flexitouch Plus | DS 3U-AS-L2-R | FDA UDI | Class II | Active |
| Flexitouch Plus | PD32-G3 DEV14 | FDA UDI | Class II | Active |
| Flexitouch Plus | DS 3L-FL-XW-R | FDA UDI | Class II | Active |
| Flexitouch Plus | DS 3U-AR-WD-R | FDA UDI | Class II | Active |
| nimbl | PL-AR-SH-LR | FDA UDI | Class II | Active |
| Airwear Air Compression Wrap | AW-XL-01-BK | FDA UDI | Class I | Unknown |
| Flexitouch | U-AS-L3-L | FDA UDI | Class II | Active |
| ACTitouch | R 500234-000-00 | FDA UDI | Class II | Unknown |
| Flexitouch | LE32T18L | FDA UDI | Class II | Active |
| Flexitouch Plus | 300007-000-00 | FDA UDI | Class II | Active |
| Flexitouch Plus | PD32-G3 | FDA UDI | Class II | Active |
| ACTitouch | 500224-000-00 | FDA UDI | Class II | Unknown |
| Flexitouch | L-TR-XT-R | FDA UDI | Class II | Active |
| ACTitouch | DS 500222-100-00 | FDA UDI | Class II | Unknown |
| Flexitouch Plus | DS 3U-AS-S1-R | FDA UDI | Class II | Active |
| Flexitouch Plus | 3L-FL-SW-R | FDA UDI | Class II | Active |
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