← Back to catalogue

Recap-it

FDA UDI

Class II (US FDA UDI)

by Doc Brands, Inc.

Identity

Trade Name
Recap-it FDA UDI
Generic Name
Home-use dental cement FDA UDI
Device Name
Recapit is a Eugenol free temporary dental cement for re-cementing loose caps or crowns. FDA UDI
Model / Reference
1 FDA UDI
Description
Recapit is a Eugenol free temporary dental cement for re-cementing loose caps or crowns. FDA UDI

Identifiers

Primary DI / UDI-DI
00372494101700 FDA UDI
510(k) Number
K964773 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Home-use dental cement FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Home-use dental cement

Recap-it by Doc Brands, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use dental cement.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Doc Brands, Inc.

Sources (1)

  • FDA UDI 66bf0e43-7060-48c0-b08c-028698f2f434 35 fields · synced Jun 1, 2026