Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “Palatal Arch”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
28
FDA 510(k) incl. De Novo
FDA PMA
GUDID
43
Country / market
European Union (all)
28
United States
43
More countries (1)
Netherlands
28
Risk class
Class I
15
Class IIa
28
Class IIb
Class III
Class II (US)
More classes (11)
Class A
Class B
Class C
Class D
IVD General
IVD Annex II List A
IVD Annex II List B
IVD for self-testing
Active implantable (AIMDD)
Unclassified (FDA)
Not classified (FDA)
Verified
Verified only
Category (EMDN)
Browse by category
Apply filters
43 devices found
·
sorted by relevance
Key
Clear all
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Niti Palatal Expander 271-450
Ortho Arch Company Inc
·
,
FDA registration: United States
GUDID
on market
None
Registry:
GUDID
Class
Class:
I
Niti Palatal Expander 271-458
Ortho Arch Company Inc
·
,
FDA registration: United States
GUDID
on market
None
Registry:
GUDID
Class
Class:
I
Niti Palatal Expander 271-452
Ortho Arch Company Inc
·
,
FDA registration: United States
GUDID
on market
None
Registry:
GUDID
Class
Class:
I
Previous
Next
Showing 41-43 of 43