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Zyppah

FDA UDI

Class II (US FDA UDI)

by A.m.a. Plastics

Identity

Trade Name
Zyppah FDA UDI
Generic Name
Mandible-repositioning sleep-disordered breathing orthosis FDA UDI
Device Name
Hybrid oral appliance, marbled pink / pink / white version FDA UDI
Model / Reference
Marbled Pink FDA UDI
Description
Hybrid oral appliance, marbled pink / pink / white version FDA UDI

Identifiers

Catalog Number
ZCA-100-05 FDA UDI
Primary DI / UDI-DI
00866868000336 FDA UDI
FDA Product Code
LRK FDA UDI
GMDN Term
Mandible-repositioning sleep-disordered breathing orthosis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mandible-repositioning sleep-disordered breathing orthosis

Zyppah by A.m.a. Plastics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mandible-repositioning sleep-disordered breathing orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A.m.a. Plastics

Sources (1)

  • FDA UDI 26fbb5cc-09c4-4896-a351-f8b483c802ab 35 fields · synced May 30, 2026