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Dukal LLC

US

Last updated September 17, 2026

Information

Country
US
Address
2 Fleetwood Ct., Ronkonkoma, NY, 11779
Website
dukal.com
LinkedIn
—
Facebook
—
Phone
+1(631)656-3800
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
1000137528
DUNS Number
791014871

Catalogue (792)

Page 13 of 16
DeviceModel / ReferenceRegistriesClassStatus
Dukal 350-10
FDA UDI
Class IActive
Dukal 27603
FDA UDI
Class IActive
American White Cross SVYJD
FDA UDI
Class IActive
Dukal 381L
FDA UDI
Class IActive
Dukal 390XL
FDA UDI
Class IUnknown
Dukal 380M
FDA UDI
Class IActive
Dukal 381XXL
FDA UDI
Class IActive
Dukal 15100
FDA UDI
Class IActive
Dukal 1414-10
FDA UDI
Class IActive
Dukal 262
FDA UDI
UActive
Dukal 453
FDA UDI
Class IActive
Dukal NLT4500
FDA UDI
Class IActive
Unipack UBC-8048
FDA UDI
Class IIActive
Dukal 375XXL
FDA UDI
Class IActive
Dukal E150
FDA UDI
Class IActive
Dukal 380XXL
FDA UDI
Class IActive
Dukal 124
FDA UDI
Class IActive
Dukal 221
FDA UDI
UActive
Tech-Med 4404M
FDA UDI
Class IActive
Tech-Med 4423M
FDA UDI
Class IActive
Dukal 403
FDA UDI
Class IActive
Dukal 2128
FDA UDI
Class IActive
Dukal 877
FDA UDI
Class IActive
Dukal 383XL
FDA UDI
Class IActive
American White Cross 1950033
FDA UDI
Class IActive
Dukal 5156
FDA UDI
Class IActive
Tech-Med 4260
FDA UDI
Class IActive
Dukal CT-01B
FDA UDI
Class IActive
Dukal 27607
FDA UDI
Class IActive
Dukal 330
FDA UDI
Class IUnknown
Tech-Med 4351BLK
FDA UDI
Class IActive
Dukal 8220
FDA UDI
Class IActive
Dukal 7608
FDA UDI
Class IActive
Dukal 270
FDA UDI
UActive
Dukal 392XL
FDA UDI
Class IActive
Dukal 341P
FDA UDI
Class IActive
Dukal 309XL-GSS
FDA UDI
Class IUnknown
Dukal 321B
FDA UDI
Class IActive
Dukal AT2323
FDA UDI
Class IActive
Dukal CT-08B
FDA UDI
Class IActive
Tech-Med 4261
FDA UDI
Class IActive
Dukal 10-1836-3
FDA UDI
Class IActive
Dukal CT-04W
FDA UDI
Class IActive
Dukal C83082
FDA UDI
Class IActive
Tech-Med 2010C
FDA UDI
Class IIActive
Dukal 1087756
FDA UDI
Class IActive
Dukal 1542
FDA UDI
Class IIActive
Tech-Med 1100BL
FDA UDI
Class IActive
Dukal 6412
FDA UDI
Class IActive
Dukal 205-12
FDA UDI
UActive

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Importers

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Authorities

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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
Jun 1, 2017Z-0233-2018—terminated

Intact carton revealed presence of shredded burn sheets