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Peeso Reamers 671541

by Tulsa Dental Products LLC

Peeso Reamers 671541 is a Class I device made by Tulsa Dental Products LLC, listed in FDA GUDID since 26 Oct 2022 (UDI-DI D7166715411), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD7166715411 UDI-DI Date26 Oct 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Peeso Reamers
Generic name
Rotary/reciprocating endodontic file/rasp, single-use
Model / Ref / Catalog
671541
Primary DI / UDI-DI
D7166715411
FDA product code
EKP
GMDN term
Rotary/reciprocating endodontic file/rasp, single-use
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rotary/reciprocating endodontic file/rasp, single-use

Similar devices in this category

Other devices filed under Rotary/reciprocating endodontic file/rasp, single-use.

Other devices from Tulsa Dental Products LLC

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Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)