Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Oxford Performance Materials

US

Last updated May 23, 2026

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
—

Catalogue (4478)

Page 90 of 90
DeviceModel / ReferenceRegistriesClassStatus
Htr-Pekk PK626593
FDA UDI
Class IIActive
Htr-Pekk PK619784
FDA UDI
Class IIActive
Htr-Pekk PK623565
FDA UDI
Class IIActive
Htr-Pekk PK618654
FDA UDI
Class IIActive
Htr-Pekk PK617703
FDA UDI
Class IIActive
Htr-Pekk PK617381
FDA UDI
Class IIActive
Htr-Pekk PK625821
FDA UDI
Class IIActive
Htr-Pekk PK624146
FDA UDI
Class IIActive
Htr-Pekk PK621592
FDA UDI
Class IIActive
Htr-Pekk PK626863
FDA UDI
Class IIActive
Htr-Pekk PK618171
FDA UDI
Class IIActive
Htr-Pekk PK618910
FDA UDI
Class IIActive
Htr-Pekk PK618533
FDA UDI
Class IIActive
Htr-Pekk PK619543
FDA UDI
Class IIActive
Htr-Pekk PK619257
FDA UDI
Class IIActive
Htr-Pekk PK625774
FDA UDI
Class IIActive
Htr-Pekk PK625654
FDA UDI
Class IIActive
Htr-Pekk PK621184
FDA UDI
Class IIActive
Htr-Pekk PK620794
FDA UDI
Class IIActive
Htr-Pekk PK620627
FDA UDI
Class IIActive
Htr-Pekk PK620897
FDA UDI
Class IIActive
Htr-Pekk PK625896
FDA UDI
Class IIActive
Osteofab Patient Specific Facial Device K133809
FDA 510(k)
Class IIActive
SpineFab Vertebral Body Replacement (VBR) System K142005
FDA 510(k)
Class IIActive
OsteoFab Patient Specific Cranial Device K180064
FDA 510(k)
Class IIActive
OsteoFab Patient Specific Facial Device K161052
FDA 510(k)
Class IIActive
Osteofab Patient Specific Cranial Device K121818
FDA 510(k)
Class IIActive
OsteoFab Suture Anchors K190915
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.