← Back to catalogue

PDT, Inc.

FDA UDI

Class I (US FDA UDI)

by PDT, Inc.

Identity

Trade Name
PDT, Inc. FDA UDI
Generic Name
Dental spatula, reusable FDA UDI
Device Name
Kit Includes: (T009D-L) D-Series FlipTop™ Cassette - LiftOut Rack 9 (R166) 5 Explorer (R245) Cone Socket Mirror Handle (R286) G2 Thin Composite (R287) G3 Thin Composite (R362) 113 Off Angle Cord Packer (R375) Mixing Spatula-Applicator (R386) 38-39 Excavator (R534) IPC-T Gold Line™ (Composite Sculpting System) (T042) Meriam Tweezers (T046) Miller Articulating Paper Forceps (T050) #5 Mirror (15/16") (T235) Aspirating Anesthetic Syringe Medium (T800) Iris Curved Scissors (11.5cm) FDA UDI
Model / Reference
R934 PDT Composite & Crown Prep Kit FDA UDI
Description
Kit Includes: (T009D-L) D-Series FlipTop™ Cassette - LiftOut Rack 9 (R166) 5 Explorer (R245) Cone Socket Mirror Handle (R286) G2 Thin Composite (R287) G3 Thin Composite (R362) 113 Off Angle Cord Packer (R375) Mixing Spatula-Applicator (R386) 38-39 Excavator (R534) IPC-T Gold Line™ (Composite Sculpting System) (T042) Meriam Tweezers (T046) Miller Articulating Paper Forceps (T050) #5 Mirror (15/16") (T235) Aspirating Anesthetic Syringe Medium (T800) Iris Curved Scissors (11.5cm) FDA UDI

Identifiers

Catalog Number
R934 FDA UDI
Primary DI / UDI-DI
00813677024954 FDA UDI
FDA Product Code
EKC FDA UDI
EAX FDA UDI
FSM FDA UDI
EKB FDA UDI
EJB FDA UDI
EKH FDA UDI
DZN FDA UDI
EJY FDA UDI
EIC FDA UDI
EGN FDA UDI
GMDN Term
Dental spatula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
878.4800 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Instrument tray, reusableSurgical soft-tissue manipulation forceps, tweezers-like, reusableDental surgical probe, reusableDental mirror, reusable

PDT, Inc. by PDT, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord packing tool.

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
PDT, Inc.

Sources (1)

  • FDA UDI cc6edef4-5193-49ce-8ab9-791eb1df0a52 34 fields · synced Jun 9, 2026