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TIDI PRODUCTS, LLC

United States·US-MF-000012287

Last updated September 17, 2026

Information

Country
United States
Address
570, Enterprise Drive, Neenah, United States
LinkedIn
—
Facebook
—
Phone
1-920-751-4300 x 4009
PRRC Contact
Chris Rahn
EUDAMED SRN
US-MF-000012287
FDA FEI Number
2182318
DUNS Number
—

Catalogue (2730)

Page 55 of 55
DeviceModel / ReferenceRegistriesClassStatus
Gems 25932
FDA UDI
Class IIUnknown
Oec 21184
FDA UDI
Class IIActive
Drapetech 30057
FDA UDI
Class IUnknown
HeffMed 28115
FDA UDI
Class IIUnknown
Sirona 20809
FDA UDI
Class IActive
Oec 20765
FDA UDI
Class IIUnknown
Medi-Inn MICK-16738-BULK
FDA UDI
Class IIUnknown
Mizuho Osi 22826
FDA UDI
Class IIUnknown
AquaGuard 50010-RBX
FDA UDI
Class IActive
Bone Foam 25187
FDA UDI
Class IIUnknown
Omnisorb 942022
FDA UDI
Class IActive
Biocommerciale 29655
FDA UDI
Class IIUnknown
GE Healthcare 24846
FDA UDI
Class IUnknown
Skytron 24606
FDA UDI
Class IIActive
Idi 25340
FDA UDI
Class IIUnknown
Posey 8235NCHH
FDA UDI
Class IUnknown
Bone Foam 31329
FDA UDI
Class IIUnknown
Medi-Inn MICK-1822-BULK
FDA UDI
Class IIUnknown
Vital Care 27344
FDA UDI
Class IIUnknown
PenBlade PB-M-15
FDA UDI
Class IActive
Dornier MedTech Europe 26064
FDA UDI
Class IIUnknown
Venture 260002
FDA UDI
Class IUnknown
Medi-Inn MICK-P696
FDA UDI
Class IIUnknown
Gems 20810F
FDA UDI
Class IIUnknown
Vital Care 23349
FDA UDI
Class IIUnknown
Tidisheild K132953
FDA 510(k)
Class IIActive
Tidi Facemask K092580
FDA 510(k)
Class IIActive
Tidi Facemask K100800
FDA 510(k)
Class IIActive
General - non-sterile 5406
EUDAMEDFDA UDI
Class IActive
General - non-sterile 5421
EUDAMEDFDA UDI
Class IActive

Related Companies

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Apr 12, 2019Z-0194-2020—terminated

Not meeting design specifications.