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Meta Biomed, Inc.

US

Last updated September 17, 2026

Part of Meta Biomed Co., Ltd.

What Meta Biomed, Inc. makes

Meta Biomed, Inc. manufactures endodontic paper points, synthetic gutta-percha, rotary and reciprocating endodontic files and rasps, dental composite resins, animal-derived dental bone matrix implants, endodontic temporary cements, tungsten-weighted oesophageal dilators, and hygroscopic dental cements.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA's Global Unique Device Identification Database (GUDID). Meta Biomed, Inc. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Meta Biomed, Inc. manufacture?

Meta Biomed, Inc. manufactures endodontic paper points, synthetic gutta-percha, rotary and reciprocating endodontic files and rasps, dental composite resins, animal-derived dental bone matrix implants, endodontic temporary cements, tungsten-weighted oesophageal dilators, and hygroscopic dental cements. These products are listed in the device categories provided, and the company does not produce any other types of devices beyond those specified in the data.

Where is Meta Biomed, Inc. based?

Meta Biomed, Inc. is based in the United States, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field confirms this location, and no other geographic details about the company's headquarters or facilities are provided or implied.

In which regulatory registry are Meta Biomed, Inc.'s devices listed?

Meta Biomed, Inc.'s devices are listed in the FDA's Global Unique Device Identification Database (GUDID), which is referenced in the LISTED IN field as 'fda_udi' and confirmed in the SUMMARY. This registry is used for tracking medical devices in the U.S. market, and the company's inclusion there does not imply approval or clearance of any device.

How are Meta Biomed, Inc.'s devices classified under regulatory frameworks?

Meta Biomed, Inc.'s devices are classified as Class I and Class II medical devices, as stated in the DEVICE CLASSES field and reiterated in the SUMMARY. This classification reflects the level of regulatory control required, with Class I being low risk and Class II requiring special controls, but it does not indicate that the company itself is approved or cleared.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
3015 Advance Lane, Colmar, PA, 18915
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3007301326
DUNS Number
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Catalogue (1566)

Page 6 of 32
DeviceModel / ReferenceRegistriesClassStatus
Mx 04-40 1471
FDA UDI
Class IActive
Absorbent Paper Points, 06-LM-15/40 2715
FDA UDI
Class IActive
Absorbent Paper Points, 90/140 2626
EUDAMEDFDA UDI
Class IActive
Absorbent Paper Points, 04-20 2662
FDA UDI
Class IActive
Absorbent Paper Points M 2764
FDA UDI
Class IActive
Absorbent Paper Points, 06-LM-15/40 2343
FDA UDI
Class IActive
Aurum (Blue Asst 31mm) 5043
FDA UDI
Class IActive
Absorbent Paper Points, LM-90/140 2419
FDA UDI
Class IActive
Gutta Percha 02-100 0815
FDA UDI
Class IActive
Absorbent Paper Points, 06-LM-15/40 2486
FDA UDI
Class IActive
Gutta Percha 02-80 0417
EUDAMEDFDA UDI
Class IActive
Gutta Percha 02-110 0698
FDA UDI
Class IActive
Metacem Kit 9404
FDA UDI
Class IIActive
Absorbent Paper Points, 130 2393
FDA UDI
Class IActive
Absorbent Paper Points, 06-LM-45 2709
FDA UDI
Class IActive
Gutta Percha 04-35 0749
FDA UDI
Class IActive
Gutta Percha 04-LM-80 0621
FDA UDI
Class IActive
NexPost Drill (NPD-2.2) 9402
FDA UDI
Class IUnknown
Gutta Percha 06-LM-70 0915
FDA UDI
Class IActive
Absorbent Paper Points, LM-15 2518
FDA UDI
Class IActive
Absorbent Paper Points, LM-C 2430
FDA UDI
Class IActive
Absorbent Paper Points, 90/140 2865
FDA UDI
Class IActive
Absorbent Paper Points, LM-120 2882
FDA UDI
Class IActive
Aurum (Pro F1 Refill 31mm) 5071
FDA UDI
Class IActive
BoneMedik, 10X20X50mm 9503
FDA UDI
Class IIUnknown
Absorbent Paper Points, 06-LM-80 2485
FDA UDI
Class IActive
Absorbant Paper Points, 130 2734
FDA UDI
Class IActive
Absorbent Paper Points, LM-140 2645
FDA UDI
Class IActive
Gutta Percha 04-15 0863
FDA UDI
Class IActive
Gutta Percha 04-LM-20 0774
FDA UDI
Class IActive
BoneMedik-DM, 0.1~0.3mm, 10cc 9735
FDA UDI
Class IIActive
BoneMedik-DM, 1~2mm, 5cc 9752
FDA UDI
Class IIActive
Absorbant Paper Points, 20 2497
FDA UDI
Class IActive
Absorbent Paper Points, 06-45 2309
FDA UDI
Class IActive
Absorbent Paper Points, 06-80 2314
FDA UDI
Class IActive
Gutta Percha 02-70 0416
EUDAMEDFDA UDI
Class IActive
Aurum (Blue T2.5 Refill 21mm) 5090
FDA UDI
Class IActive
Absorbent Paper Points, NC 10 2577
FDA UDI
Class IActive
Gutta Percha 02-LM-50 0831
FDA UDI
Class IActive
Gutta Percha LM-R-ML 0742
FDA UDI
Class IActive
Absorbent Paper Points, LM-60 2839
FDA UDI
Class IActive
Absorbent Paper Points, LM-130 2272
FDA UDI
Class IActive
Absorbent Paper Points, LM-30 2870
FDA UDI
Class IActive
Absorbent Paper Points, 110 2620
FDA UDI
Class IActive
Gutta Percha 06-LM-30 0628
FDA UDI
Class IActive
Nexcomp Set 9455
FDA UDI
Class IIActive
Aurum Blue T4 Absorbent Paper Points, LM-04-40 2563
FDA UDI
Class IActive
Gutta Percha 04-50 0870
FDA UDI
Class IActive
Nexcomp flow TL 9257
FDA UDI
Class IIActive
Absorbent Paper Points, 06-15/40 2315
FDA UDI
Class IActive

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